A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012934



Internal ID19102151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5534522..5568113hg38UCSC Ensembl
Innerchr4:5536249..5569840hg19UCSC Ensembl
Innerchr4:5587150..5620741hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3833592
hg1933592
hg1833592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616180
Samples
Known GenesEVC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012934
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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