A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524859



Internal ID15452152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69708654..69837725hg38UCSC Ensembl
InnerchrX:68928498..69057567hg19UCSC Ensembl
InnerchrX:68845223..68974292hg18UCSC Ensembl
InnerchrX:68711519..68840588hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38129072
hg19129070
hg18129070
hg17129070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700863
Samples
Known GenesEDA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524859
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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