A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490662



Internal ID19078303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196819844..196947657hg38UCSC Ensembl
Innerchr1:196788974..196916787hg19UCSC Ensembl
Innerchr1:195055597..195183410hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38127814
hg19127814
hg18127814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997545
Supporting Variants
Samples
Known GenesCFHR1, CFHR2, CFHR4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3490662
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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