A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526140



Internal ID15453433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:170873133..170875987hg38UCSC Ensembl
Innerchr2:171729643..171732497hg19UCSC Ensembl
Innerchr2:171437889..171440743hg18UCSC Ensembl
Innerchr2:171555150..171558004hg17UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382855
hg192855
hg182855
hg172855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702395
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526140
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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