A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091194



Internal ID15944380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95349767..95351896hg38UCSC Ensembl
Innerchr7:94979079..94981208hg19UCSC Ensembl
Innerchr7:94817015..94819144hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382130
hg192130
hg182130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607861
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)nssv1091194
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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