A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493959



Internal ID19081600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196771830..196843388hg38UCSC Ensembl
Innerchr1:196740960..196812518hg19UCSC Ensembl
Innerchr1:195007583..195079141hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3871559
hg1971559
hg1871559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002413
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)nssv3493959
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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