A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620646



Internal ID18918927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32458857..32514244hg38UCSC Ensembl
Innerchr4:32460479..32515866hg19UCSC Ensembl
Innerchr4:32104377..32159764hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3855388
hg1955388
hg1855388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003745
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)nssv3620646
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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