A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585174



Internal ID16372583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:599013..614136hg38UCSC Ensembl
Innerchr20:579657..594780hg19UCSC Ensembl
Innerchr20:527657..542780hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3815124
hg1915124
hg1815124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7421n54
Supporting Variantsnssv1150942
Samples1780862574_A
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585174
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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