A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv790062



Internal ID16084018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27779963..27780611hg38UCSC Ensembl
Innerchr12:27932896..27933544hg19UCSC Ensembl
Innerchr12:27824163..27824811hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38649
hg19649
hg18649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557847
Supporting Variants
Samples
Known GenesKLHL42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv790062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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