A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3494778



Internal ID19082419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196745680..196798270hg38UCSC Ensembl
Innerchr1:196714810..196767400hg19UCSC Ensembl
Innerchr1:194981433..195034023hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3852591
hg1952591
hg1852591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008005
Supporting Variants
Samples
Known GenesCFH, CFHR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3494778
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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