A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005097



Internal ID19094314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32386962..32429951hg38UCSC Ensembl
Innerchr4:32388584..32431573hg19UCSC Ensembl
Innerchr4:32032482..32075471hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3842990
hg1942990
hg1842990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5164n100
Supporting Variantsnssv3620643
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)nsv1005097
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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