A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585178



Internal ID16025901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:607445..613017hg38UCSC Ensembl
Innerchr20:588089..593661hg19UCSC Ensembl
Innerchr20:536089..541661hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385573
hg195573
hg185573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7422n54
Supporting Variantsnssv935234
Samples
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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