A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520535



Internal ID15447828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121607830..121820265hg38UCSC Ensembl
InnerchrX:120741684..120954118hg19UCSC Ensembl
InnerchrX:120569365..120781799hg18UCSC Ensembl
InnerchrX:120467219..120679653hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38212436
hg19212435
hg18212435
hg17212435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv529n21
Supporting Variantsnssv672257, nssv691839, nssv689476
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520535
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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