A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579440



Internal ID16020163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36354250..36354635hg38UCSC Ensembl
Innerchr19:36845152..36845537hg19UCSC Ensembl
Innerchr19:41536992..41537377hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38386
hg19386
hg18386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899102
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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