A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655059



Internal ID18606654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5709351..5879467hg38UCSC Ensembl
Innerchr7:5748982..5919098hg19UCSC Ensembl
Innerchr7:5715508..5885624hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38170117
hg19170117
hg18170117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028601
Supporting Variants
Samples
Known GenesMIR6874, RNF216, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655059
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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