A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527009



Internal ID15454302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75121920..75128354hg38UCSC Ensembl
Innerchr2:75349046..75355480hg19UCSC Ensembl
Innerchr2:75202554..75208988hg18UCSC Ensembl
Innerchr2:75260701..75267135hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg386435
hg196435
hg186435
hg176435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703384
Samples
Known GenesTACR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527009
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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