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nsv5486110

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,518

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 382 SVs from 41 studies. See in: genome view    
Submitted genomic17,893,503-17,895,020Question Mark
Overlapping variant regions from other studies: 382 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):17,751,012-17,752,529Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486110Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr817,893,50317,895,020
nsv5486110RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr817,751,01217,752,529

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17007553deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17007553Submitted genomicNC_000008.11:g.178
93503_17895020del
GRCh38 (hg38)NC_000008.11Chr817,893,50317,895,020
nssv17007553RemappedPerfectNC_000008.10:g.177
51012_17752529del
GRCh37.p13First PassNC_000008.10Chr817,751,01217,752,529

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)
nssv170075530.095746404
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