A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585912



Internal ID16373321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:31891437..31934129hg38UCSC Ensembl
Innerchr20:30479240..30521932hg19UCSC Ensembl
Innerchr20:29942901..29985593hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3842693
hg1942693
hg1842693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939256
Samples
Known GenesTTLL9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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