A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887256



Internal ID16181212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71576503..71652143hg38UCSC Ensembl
Innerchr18:69243739..69319379hg19UCSC Ensembl
Innerchr18:67394719..67470359hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3875641
hg1975641
hg1875641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577594
Supporting Variants
Samples
Known GenesLOC100505776
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887256
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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