A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000822



Internal ID18743353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14334356..14696137hg38UCSC Ensembl
Innerchr4:14335980..14697761hg19UCSC Ensembl
Innerchr4:13945078..14306859hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38361782
hg19361782
hg18361782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5144n100
Supporting Variantsnssv3619837
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)nsv1000822
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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