A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642915



Internal ID18594510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10673231..11457158hg38UCSC Ensembl
Innerchr7:10712858..11496785hg19UCSC Ensembl
Innerchr7:10679383..11463310hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38783928
hg19783928
hg18783928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019888
Supporting Variants
Samples
Known GenesNDUFA4, PHF14, THSD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642915
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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