A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662030



Internal ID18960311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112791348..112836701hg38UCSC Ensembl
Innerchr7:112431403..112476756hg19UCSC Ensembl
Innerchr7:112218639..112263992hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3845354
hg1945354
hg1845354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031405
Supporting Variants
Samples
Known GenesC7orf60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3662030
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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