A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150596



Internal ID15879286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:52830052..53096534hg38UCSC Ensembl
Innerchr18:50356422..50622904hg19UCSC Ensembl
Innerchr18:48610420..48876902hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38266483
hg19266483
hg18266483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576937
Supporting Variants
SamplesHGDP01339
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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