A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089566



Internal ID15942752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89928571..90060961hg38UCSC Ensembl
Innerchr7:89557885..89690275hg19UCSC Ensembl
Innerchr7:89395821..89528211hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38132391
hg19132391
hg18132391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607775
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)nssv1089566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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