A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522362



Internal ID15449655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31776837..31828359hg38UCSC Ensembl
Innerchr12:31929771..31981293hg19UCSC Ensembl
Innerchr12:31821038..31872560hg18UCSC Ensembl
Innerchr12:31821038..31872560hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3851523
hg1951523
hg1851523
hg1751523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694159
Samples
Known GenesH3F3C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522362
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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