A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150630



Internal ID15873501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73113514..73229094hg38UCSC Ensembl
Innerchr18:70780749..70896329hg19UCSC Ensembl
Innerchr18:68931729..69047309hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38115581
hg19115581
hg18115581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577645
Supporting Variants
SamplesHGDP00218
Known GenesLOC400655
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150630
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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