A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620674



Internal ID18918955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34839898hg38UCSC Ensembl
Innerchr4:34761520..34841520hg19UCSC Ensembl
Innerchr4:34437915..34517915hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3880001
hg1980001
hg1880001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011508
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)nssv3620674
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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