A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579429



Internal ID16020152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36352224..36353530hg38UCSC Ensembl
Innerchr19:36843126..36844432hg19UCSC Ensembl
Innerchr19:41534966..41536272hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381307
hg191307
hg181307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6425n54
Supporting Variantsnssv898990, nssv898989
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579429
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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