A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585325



Internal ID16026048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5261913..5504492hg38UCSC Ensembl
Innerchr20:5242559..5485138hg19UCSC Ensembl
Innerchr20:5190559..5433138hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38242580
hg19242580
hg18242580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937454
Samples
Known GenesLINC00654, LINC00658, LOC643406, PROKR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585325
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer