A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv787447



Internal ID15734717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8697754..8698721hg38UCSC Ensembl
Innerchr12:8850350..8851317hg19UCSC Ensembl
Innerchr12:8741617..8742584hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38968
hg19968
hg18968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557349
Supporting Variants
Samples
Known GenesRIMKLB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv787447
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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