A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516563



Internal ID15443856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93249161..93461201hg38UCSC Ensembl
InnerchrX:92504160..92716200hg19UCSC Ensembl
InnerchrX:92390816..92602856hg18UCSC Ensembl
InnerchrX:92310305..92522345hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38212041
hg19212041
hg18212041
hg17212041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704156, nssv669180, nssv697303, nssv658585, nssv700145, nssv672609, nssv703698, nssv678487, nssv670218
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516563
Frequency
Sample Size2026
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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