nsv1722

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,851

Genome View

Select assembly:
Overlapping variant regions from other studies: 311 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):5,031,097-5,075,947Question Mark
Overlapping variant regions from other studies: 311 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):5,081,098-5,125,948Question Mark
Overlapping variant regions from other studies: 19 SVs from 8 studies. See in: genome view    
Submitted genomic5,021,099-5,065,949Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv1722RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr165,031,0975,075,947
nsv1722RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr165,081,0985,125,948
nsv1722Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000016.8Chr165,021,0995,065,949

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv7227deletionNA12156SequencingPaired-end mapping3,265

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv7227RemappedPerfectNC_000016.10:g.(50
31097_?)_(?_507594
7)del
GRCh38.p12First PassNC_000016.10Chr165,031,0975,075,947
nssv7227RemappedPerfectNC_000016.9:g.(508
1098_?)_(?_5125948
)del
GRCh37.p13First PassNC_000016.9Chr165,081,0985,125,948
nssv7227Submitted genomicNC_000016.8:g.(502
1099_?)_(?_5065949
)del5410
NCBI35 (hg17)NC_000016.8Chr165,021,0995,065,949

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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