A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528492



Internal ID15455785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:4352995..4364163hg38UCSC Ensembl
Innerchr12:4462161..4473329hg19UCSC Ensembl
Innerchr12:4332422..4343590hg18UCSC Ensembl
Innerchr12:4332422..4343590hg17UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3811169
hg1911169
hg1811169
hg1711169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705097
Samples
Known GenesC12orf5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528492
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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