A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493454



Internal ID19081095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:181134873..181168684hg38UCSC Ensembl
Innerchr1:181104009..181137820hg19UCSC Ensembl
Innerchr1:179370632..179404443hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3833812
hg1933812
hg1833812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007439
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3493454
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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