A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv787442



Internal ID15734712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8697754..8698670hg38UCSC Ensembl
Innerchr12:8850350..8851266hg19UCSC Ensembl
Innerchr12:8741617..8742533hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38917
hg19917
hg18917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557348
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)nssv787442
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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