A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661698



Internal ID18959979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62506780..62944328hg38UCSC Ensembl
Innerchr7:61846306..62404706hg19UCSC Ensembl
Innerchr7:61483741..62042141hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38437549
hg19558401
hg18558401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016125
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661698
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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