A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523145



Internal ID15450438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:156640351..156646004hg38UCSC Ensembl
Innerchr2:157496863..157502516hg19UCSC Ensembl
Innerchr2:157205109..157210762hg18UCSC Ensembl
Innerchr2:157322371..157328024hg17UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg385654
hg195654
hg185654
hg175654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698853
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523145
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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