A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519792



Internal ID15100399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:94357807..94989222hg38UCSC Ensembl
InnerchrX:93612806..94244221hg19UCSC Ensembl
InnerchrX:93499462..94130877hg18UCSC Ensembl
InnerchrX:93418951..94050366hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38631416
hg19631416
hg18631416
hg17631416
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658666, nssv690300, nssv696689, nssv697129, nssv685411, nssv673464, nssv706003, nssv661264
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519792
Frequency
Sample Size2026
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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