A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898989



Internal ID15846259
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 StatusS
Merged Variantsnsv579429
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)nssv898989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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