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nsv5421580

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:245,240

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1298 SVs from 106 studies. See in: genome view    
Submitted genomic152,489,543-152,734,782Question Mark
Overlapping variant regions from other studies: 1310 SVs from 107 studies. See in: genome view    
Remapped(Score: Perfect):152,462,019-152,707,258Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5421580Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1152,489,543152,734,782
nsv5421580RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1152,462,019152,707,258

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16891214duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16891214Submitted genomicNC_000001.11:g.152
489543_152734782du
p
GRCh38 (hg38)NC_000001.11Chr1152,489,543152,734,782
nssv16891214RemappedPerfectNC_000001.10:g.152
462019_152707258du
p
GRCh37.p13First PassNC_000001.10Chr1152,462,019152,707,258

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)
nssv16891214<0.00126404
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