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nsv5510426

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,945

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 30 studies. See in: genome view    
Submitted genomic42,784,507-42,790,451Question Mark
Overlapping variant regions from other studies: 128 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):43,076,705-43,082,649Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5510426Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1542,784,50742,790,451
nsv5510426RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1543,076,70543,082,649

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699803deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699803Submitted genomicNC_000015.10:g.427
84507_42790451del
GRCh38 (hg38)NC_000015.10Chr1542,784,50742,790,451
nssv17699803RemappedPerfectNC_000015.9:g.4307
6705_43082649del
GRCh37.p13First PassNC_000015.9Chr1543,076,70543,082,649

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)
nssv17699803<0.00116404
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