A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1079633



Internal ID15586133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16875904..17375160hg38UCSC Ensembl
Innerchr7:16915528..17414784hg19UCSC Ensembl
Innerchr7:16882053..17381309hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38499257
hg19499257
hg18499257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606342
Supporting Variants
Samples
Known GenesAGR3, AHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1079633
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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