A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586178



Internal ID16373587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:50838374..50876634hg38UCSC Ensembl
Innerchr20:49454911..49493171hg19UCSC Ensembl
Innerchr20:48888318..48926578hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3838261
hg1938261
hg1838261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv940984
Samples
Known GenesBCAS4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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