nsv5400977

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 25 studies. See in: genome view    
Submitted genomic94,784,137-94,784,152Question Mark
Overlapping variant regions from other studies: 109 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):94,517,303-94,517,318Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5400977Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1194,784,13794,784,152
nsv5400977RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1194,517,30394,517,318

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17050006alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17050006Submitted genomicNC_000011.10:g.947
84137_94784152ins2
80
GRCh38 (hg38)NC_000011.10Chr1194,784,13794,784,152
nssv17050006RemappedPerfectNC_000011.9:g.9451
7303_94517318ins28
0
GRCh37.p13First PassNC_000011.9Chr1194,517,30394,517,318

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv170500060.005306404
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