A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528353



Internal ID15108960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:22914368..23525618hg38UCSC Ensembl
Innerchr12:23067302..23678552hg19UCSC Ensembl
Innerchr12:22958569..23569819hg18UCSC Ensembl
Innerchr12:22958569..23569819hg17UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38611251
hg19611251
hg18611251
hg17611251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv91n21
Supporting Variantsnssv704938
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528353
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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