A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524161



Internal ID15451454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138351859..138448461hg38UCSC Ensembl
InnerchrX:137434018..137530619hg19UCSC Ensembl
InnerchrX:137261684..137358285hg18UCSC Ensembl
InnerchrX:137159538..137256139hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3896603
hg1996602
hg1896602
hg1796602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700040
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524161
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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