A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060112



Internal ID18802643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9552450..9699217hg38UCSC Ensembl
Innerchr19:9663126..9809893hg19UCSC Ensembl
Innerchr19:9524126..9670893hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38146768
hg19146768
hg18146768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723281
Samples
Known GenesC19orf82, ZNF121, ZNF561, ZNF562, ZNF812
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060112
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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