A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586370



Internal ID16373779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59877146..59892746hg38UCSC Ensembl
Innerchr20:58452201..58467801hg19UCSC Ensembl
Innerchr20:57885596..57901196hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3815601
hg1915601
hg1815601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941813
Samples
Known GenesSYCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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