A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579857



Internal ID16367266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44424713..44430844hg38UCSC Ensembl
Innerchr19:44928885..44935019hg19UCSC Ensembl
Innerchr19:49620725..49626859hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg386132
hg196135
hg186135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899921, nssv899922
Samples
Known GenesZNF229
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579857
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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