A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606343



Internal ID16047066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17046315..17715960hg38UCSC Ensembl
Innerchr7:17085939..17755584hg19UCSC Ensembl
Innerchr7:17052464..17722109hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38669646
hg19669646
hg18669646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155307
SamplesHGDP01240
Known GenesAHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606343
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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