A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1085469



Internal ID15938655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64105575..64323008hg38UCSC Ensembl
Innerchr7:63565953..63783386hg19UCSC Ensembl
Innerchr7:63203388..63420821hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38217434
hg19217434
hg18217434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607308
Supporting Variants
Samples
Known GenesZNF679, ZNF735, ZNF736
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1085469
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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