A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083046



Internal ID15589546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40153936..40311288hg38UCSC Ensembl
Innerchr7:40193535..40350887hg19UCSC Ensembl
Innerchr7:40160060..40317412hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38157353
hg19157353
hg18157353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606710
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083046
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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