A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1087858



Internal ID15941044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75604841..75659352hg38UCSC Ensembl
Innerchr7:75234159..75288670hg19UCSC Ensembl
Innerchr7:75072095..75126606hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3854512
hg1954512
hg1854512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607510
Supporting Variants
Samples
Known GenesHIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1087858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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