A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089373



Internal ID15942559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84546973..84689167hg38UCSC Ensembl
Innerchr7:84176289..84318483hg19UCSC Ensembl
Innerchr7:84014225..84156419hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38142195
hg19142195
hg18142195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607712
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)nssv1089373
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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