A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520647



Internal ID15447940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:84510546..84708918hg38UCSC Ensembl
InnerchrX:83765554..83963926hg19UCSC Ensembl
InnerchrX:83652210..83850582hg18UCSC Ensembl
InnerchrX:83571699..83770071hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38198373
hg19198373
hg18198373
hg17198373
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695480, nssv700025, nssv690768, nssv673525, nssv696106
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520647
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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