A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091645



Internal ID15944831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99863860..99865757hg38UCSC Ensembl
Innerchr7:99461483..99463380hg19UCSC Ensembl
Innerchr7:99299419..99301316hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381898
hg191898
hg181898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607927
Supporting Variants
Samples
Known GenesCYP3A43
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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