A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3700655



Internal ID18652250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:46809229..46856310hg38UCSC Ensembl
Innerchr1:47274901..47321982hg19UCSC Ensembl
Innerchr1:47047488..47094569hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3847082
hg1947082
hg1847082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004246
Supporting Variants
Samples
Known GenesCYP4B1, CYP4Z2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3700655
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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