A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002303



Internal ID19091520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59570575..59640962hg38UCSC Ensembl
Innerchr4:60436293..60506680hg19UCSC Ensembl
Innerchr4:60118888..60189275hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3870388
hg1970388
hg1870388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626516
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)nsv1002303
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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