A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013327



Internal ID19102545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62123708..62283330hg38UCSC Ensembl
Innerchr4:62989426..63149048hg19UCSC Ensembl
Innerchr4:62672021..62831643hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38159623
hg19159623
hg18159623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739497
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)nsv1013327
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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