A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515887



Internal ID15442944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:65727482..65737283hg38UCSC Ensembl
Innerchr12:66121262..66131063hg19UCSC Ensembl
Innerchr12:64407529..64417330hg18UCSC Ensembl
Innerchr12:64407529..64417330hg17UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg389802
hg199802
hg189802
hg179802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686736, nssv674453, nssv679871, nssv675280, nssv674362, nssv665515, nssv665144, nssv658361, nssv683533
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515887
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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