A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000367



Internal ID19089584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57274438..57700455hg38UCSC Ensembl
Innerchr4:58140604..58566621hg19UCSC Ensembl
Innerchr4:57835361..58261378hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38426018
hg19426018
hg18426018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5218n100
Supporting Variantsnssv3626503
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)nsv1000367
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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