A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899136



Internal ID15846406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36354437..36357702hg38UCSC Ensembl
Innerchr19:36845339..36848604hg19UCSC Ensembl
Innerchr19:41537179..41540444hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383266
hg193266
hg183266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579453
Supporting Variants
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899136
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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