A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066792



Internal ID19156011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19829776..19889892hg38UCSC Ensembl
Innerchr19:19940585..20000701hg19UCSC Ensembl
Innerchr19:19801585..19861701hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3860117
hg1960117
hg1860117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3569790
Samples
Known GenesZNF253
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066792
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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