A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013013



Internal ID19102230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28321843..28418051hg38UCSC Ensembl
Innerchr4:28323465..28419673hg19UCSC Ensembl
Innerchr4:27932563..28028771hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3896209
hg1996209
hg1896209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737770
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)nsv1013013
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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