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nsv5501906

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:719

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 20 studies. See in: genome view    
Submitted genomic31,318,680-31,319,398Question Mark
Overlapping variant regions from other studies: 80 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):31,787,886-31,788,604Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501906Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1431,318,68031,319,398
nsv5501906RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1431,787,88631,788,604

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17693533duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17693533Submitted genomicNC_000014.9:g.3131
8680_31319398dup
GRCh38 (hg38)NC_000014.9Chr1431,318,68031,319,398
nssv17693533RemappedPerfectNC_000014.8:g.3178
7886_31788604dup
GRCh37.p13First PassNC_000014.8Chr1431,787,88631,788,604

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)
nssv17693533<0.00126404
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