A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv883295



Internal ID16177251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52511752..52574924hg38UCSC Ensembl
Innerchr18:50038122..50101294hg19UCSC Ensembl
Innerchr18:48292120..48355292hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3863173
hg1963173
hg1863173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576930
Supporting Variants
Samples
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv883295
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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