A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088539



Internal ID15941725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81241063..81318201hg38UCSC Ensembl
Innerchr7:80870379..80947517hg19UCSC Ensembl
Innerchr7:80708315..80785453hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3877139
hg1977139
hg1877139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607688
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1088539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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