A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525883



Internal ID15453176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73276075..73300903hg38UCSC Ensembl
Innerchr12:73669855..73694683hg19UCSC Ensembl
Innerchr12:71956122..71980950hg18UCSC Ensembl
Innerchr12:71956122..71980950hg17UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3824829
hg1924829
hg1824829
hg1724829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702083
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525883
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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