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nsv5505016

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,997

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
Submitted genomic6,314,207-6,321,203Question Mark
Overlapping variant regions from other studies: 90 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):6,335,437-6,342,433Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505016Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,314,2076,321,203
nsv5505016RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,335,4376,342,433

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17043254deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17043254Submitted genomicNC_000011.10:g.631
4207_6321203del
GRCh38 (hg38)NC_000011.10Chr116,314,2076,321,203
nssv17043254RemappedPerfectNC_000011.9:g.6335
437_6342433del
GRCh37.p13First PassNC_000011.9Chr116,335,4376,342,433

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)
nssv17043254<0.00116404
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