A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899594



Internal ID15846864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41896804..41902357hg38UCSC Ensembl
Innerchr19:42400893..42406507hg19UCSC Ensembl
Innerchr19:47092733..47098347hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385554
hg195615
hg185615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579625
Supporting Variants
Samples
Known GenesARHGEF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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