A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089565



Internal ID15942751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89909309..90080467hg38UCSC Ensembl
Innerchr7:89538623..89709781hg19UCSC Ensembl
Innerchr7:89376559..89547717hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38171159
hg19171159
hg18171159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607772
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)nssv1089565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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