A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3617047



Internal ID18915328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..35885hg38UCSC Ensembl
Innerchr4:12269..35885hg19UCSC Ensembl
Innerchr4:2269..25885hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3823617
hg1923617
hg1823617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007556
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)nssv3617047
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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