A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585310



Internal ID16026033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4586645..4794039hg38UCSC Ensembl
Innerchr20:4567291..4774685hg19UCSC Ensembl
Innerchr20:4515291..4722685hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38207395
hg19207395
hg18207395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937431
Samples
Known GenesPRND, PRNP, PRNT, RASSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585310
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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