A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862323



Internal ID15809593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87726878..87736098hg38UCSC Ensembl
Innerchr16:87760484..87769704hg19UCSC Ensembl
Innerchr16:86317985..86327205hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg389221
hg199221
hg189221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573537
Supporting Variants
Samples
Known GenesKLHDC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv862323
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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