A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525023



Internal ID15452316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:67279090..67314889hg38UCSC Ensembl
Innerchr12:67672870..67708669hg19UCSC Ensembl
Innerchr12:65959137..65994936hg18UCSC Ensembl
Innerchr12:65959137..65994936hg17UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3835800
hg1935800
hg1835800
hg1735800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701062
Samples
Known GenesCAND1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525023
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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