A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695807



Internal ID15432459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115105100..115105654hg38UCSC Ensembl
Innerchr12:115542905..115543459hg19UCSC Ensembl
Innerchr12:114027288..114027842hg18UCSC Ensembl
Innerchr12:114005625..114006179hg17UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38555
hg19555
hg18555
hg17555
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518378
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695807
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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