A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527640



Internal ID15454933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:113800406..113803293hg38UCSC Ensembl
Innerchr12:114238211..114241098hg19UCSC Ensembl
Innerchr12:112722594..112725481hg18UCSC Ensembl
Innerchr12:112700931..112703818hg17UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg382888
hg192888
hg182888
hg172888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704110
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527640
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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