A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658570



Internal ID15395222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5698923..5739722hg38UCSC Ensembl
InnerchrX:5616964..5657763hg19UCSC Ensembl
InnerchrX:5626964..5667763hg18UCSC Ensembl
InnerchrX:5476700..5517499hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3840800
hg1940800
hg1840800
hg1740800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515922
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658570
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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