A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078058



Internal ID15584558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1100782..1211575hg38UCSC Ensembl
Innerchr7:1140418..1251211hg19UCSC Ensembl
Innerchr7:1106944..1217737hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38110794
hg19110794
hg18110794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605735
Supporting Variants
Samples
Known GenesC7orf50, ZFAND2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078058
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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