A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155168



Internal ID15527756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37102969..37105403hg38UCSC Ensembl
Innerchr7:37142574..37145008hg19UCSC Ensembl
Innerchr7:37109099..37111533hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg382435
hg192435
hg182435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606621
Supporting Variants
SamplesHGDP00541
Known GenesELMO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155168
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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