A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607929



Internal ID16395338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99864442..99865757hg38UCSC Ensembl
Innerchr7:99462065..99463380hg19UCSC Ensembl
Innerchr7:99300001..99301316hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381316
hg191316
hg181316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11527n54
Supporting Variantsnssv1091648
Samples
Known GenesCYP3A43
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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