A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515922



Internal ID15442979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5684069..5748288hg38UCSC Ensembl
InnerchrX:5602110..5666329hg19UCSC Ensembl
InnerchrX:5612110..5676329hg18UCSC Ensembl
InnerchrX:5461846..5526065hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3864220
hg1964220
hg1864220
hg1764220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660365, nssv662874, nssv671508, nssv667540, nssv658570, nssv655834, nssv672342, nssv676513, nssv691201, nssv656831, nssv665315, nssv670357, nssv689323, nssv686015, nssv693454
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515922
Frequency
Sample Size2026
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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