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nsv5496017

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:99,263

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 431 SVs from 50 studies. See in: genome view    
Submitted genomic130,243,940-130,343,202Question Mark
Overlapping variant regions from other studies: 431 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):130,113,835-130,213,097Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496017Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11130,243,940130,343,202
nsv5496017RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11130,113,835130,213,097

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17050782deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17050782Submitted genomicNC_000011.10:g.130
243940_130343202de
l
GRCh38 (hg38)NC_000011.10Chr11130,243,940130,343,202
nssv17050782RemappedPerfectNC_000011.9:g.1301
13835_130213097del
GRCh37.p13First PassNC_000011.9Chr11130,113,835130,213,097

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)
nssv17050782<0.00116404
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