A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521524



Internal ID15448817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:26805907..26910615hg38UCSC Ensembl
InnerchrX:26824024..26928732hg19UCSC Ensembl
InnerchrX:26733945..26838653hg18UCSC Ensembl
InnerchrX:26583681..26688389hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38104709
hg19104709
hg18104709
hg17104709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698141
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521524
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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