A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607926



Internal ID16395335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99863860..99865426hg38UCSC Ensembl
Innerchr7:99461483..99463049hg19UCSC Ensembl
Innerchr7:99299419..99300985hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381567
hg191567
hg181567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11526n54
Supporting Variantsnssv1091644
Samples
Known GenesCYP3A43
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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