A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3489597



Internal ID19077238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196788663..196821901hg38UCSC Ensembl
Innerchr1:196757793..196791031hg19UCSC Ensembl
Innerchr1:195024416..195057654hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3833239
hg1933239
hg1833239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009818
Supporting Variants
Samples
Known GenesCFHR1, CFHR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3489597
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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