A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580034



Internal ID16020757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52799228..52921071hg38UCSC Ensembl
Innerchr19:53302481..53424324hg19UCSC Ensembl
Innerchr19:57994293..58116136hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38121844
hg19121844
hg18121844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150148
SamplesNINDS_240
Known GenesZNF28, ZNF320, ZNF468
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580034
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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