A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999727



Internal ID19159263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57272246..57700455hg38UCSC Ensembl
Innerchr4:58138412..58566621hg19UCSC Ensembl
Innerchr4:57833169..58261378hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38428210
hg19428210
hg18428210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5218n100
Supporting Variantsnssv3739488
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)nsv999727
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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