A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059460



Internal ID18801991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12196893..12264115hg38UCSC Ensembl
Innerchr19:12307708..12374930hg19UCSC Ensembl
Innerchr19:12168708..12235930hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3867223
hg1967223
hg1867223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3430n100
Supporting Variantsnssv3564701
Samples
Known GenesLOC100289333
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059460
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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