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nsv5510435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 32 studies. See in: genome view    
Submitted genomic114,559,681-114,559,751Question Mark
Overlapping variant regions from other studies: 110 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):114,430,403-114,430,473Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5510435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11114,559,681114,559,751
nsv5510435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11114,430,403114,430,473

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17052556deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17052556Submitted genomicNC_000011.10:g.114
559681_114559751de
l
GRCh38 (hg38)NC_000011.10Chr11114,559,681114,559,751
nssv17052556RemappedPerfectNC_000011.9:g.1144
30403_114430473del
GRCh37.p13First PassNC_000011.9Chr11114,430,403114,430,473

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)
nssv170525560.00196404
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