A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3492369



Internal ID19080010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196740618..196832930hg38UCSC Ensembl
Innerchr1:196709748..196802060hg19UCSC Ensembl
Innerchr1:194976371..195068683hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3892313
hg1992313
hg1892313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007127
Supporting Variants
Samples
Known GenesCFH, CFHR1, CFHR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3492369
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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