A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892899



Internal ID15840169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4011267..4098778hg38UCSC Ensembl
Innerchr19:4011265..4098776hg19UCSC Ensembl
Innerchr19:3962265..4049776hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3887512
hg1987512
hg1887512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578435
Supporting Variants
Samples
Known GenesMAP2K2, PIAS4, ZBTB7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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