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nsv5507750

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:149

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 66 SVs from 18 studies. See in: genome view    
Submitted genomic61,788,760-61,788,908Question Mark
Overlapping variant regions from other studies: 66 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):61,556,232-61,556,380Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507750Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1161,788,76061,788,908
nsv5507750RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1161,556,23261,556,380

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046580duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046580Submitted genomicNC_000011.10:g.617
88760_61788908dup
GRCh38 (hg38)NC_000011.10Chr1161,788,76061,788,908
nssv17046580RemappedPerfectNC_000011.9:g.6155
6232_61556380dup
GRCh37.p13First PassNC_000011.9Chr1161,556,23261,556,380

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)
nssv17046580<0.00126404
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