A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003334



Internal ID18745866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62720166..63265520hg38UCSC Ensembl
Innerchr4:63585884..64131238hg19UCSC Ensembl
Innerchr4:63268479..63813833hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38545355
hg19545355
hg18545355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5222n100
Supporting Variantsnssv3626524
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)nsv1003334
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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