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nsv6143770

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:154

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 175 SVs from 31 studies. See in: genome view    
Submitted genomic124,224,861-124,225,014Question Mark
Overlapping variant regions from other studies: 175 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):124,095,566-124,095,719Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6143770Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,224,861124,225,014
nsv6143770RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,095,566124,095,719

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053676duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053676Submitted genomicNC_000011.10:g.124
224861_124225014du
p
GRCh38 (hg38)NC_000011.10Chr11124,224,861124,225,014
nssv17053676RemappedPerfectNC_000011.9:g.1240
95566_124095719dup
GRCh37.p13First PassNC_000011.9Chr11124,095,566124,095,719

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)
nssv170536760.0533396404
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