A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579432



Internal ID16020155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36353190..36353588hg38UCSC Ensembl
Innerchr19:36844092..36844490hg19UCSC Ensembl
Innerchr19:41535932..41536330hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38399
hg19399
hg18399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899093
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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