A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv558965



Internal ID15999688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52862019..52913242hg38UCSC Ensembl
Innerchr12:53255803..53307026hg19UCSC Ensembl
Innerchr12:51542070..51593293hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3851224
hg1951224
hg1851224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv796170
Samples
Known GenesKRT8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv558965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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