A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089231



Internal ID15942417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83098134..83138383hg38UCSC Ensembl
Innerchr7:82727450..82767699hg19UCSC Ensembl
Innerchr7:82565386..82605635hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3840250
hg1940250
hg1840250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607701
Supporting Variants
Samples
Known GenesPCLO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1089231
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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