nsv4983738

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,486

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 22 studies. See in: genome view    
Submitted genomic128,155,449-128,158,935Question Mark
Overlapping variant regions from other studies: 144 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):130,917,728-130,921,214Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4983738Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9128,155,450 (-1, +1)128,158,935 (-1)
nsv4983738RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9130,917,729 (-1, +1)130,921,214 (-1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16512114deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16512114Submitted genomicNC_000009.12:g.(12
8155449_128155451)
_(128158934_?)del
GRCh38 (hg38)NC_000009.12Chr9128,155,450 (-1, +1)128,158,935 (-1)
nssv16512114RemappedPerfectNC_000009.11:g.(13
0917728_130917730)
_(130921213_?)del
GRCh37.p13First PassNC_000009.11Chr9130,917,729 (-1, +1)130,921,214 (-1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16512114<0.001129246
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