A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606621



Internal ID16047344
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 StatusM
Merged Variants
Supporting Variantsnssv1155168, nssv1155169
SamplesHGDP00541, HGDP00546
Known GenesELMO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606621
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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