A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579455



Internal ID16020178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36354506..36355281hg38UCSC Ensembl
Innerchr19:36845408..36846183hg19UCSC Ensembl
Innerchr19:41537248..41538023hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38776
hg19776
hg18776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6430n54
Supporting Variantsnssv899138, nssv899139
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579455
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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