A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586571



Internal ID16027294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63522433..63589896hg38UCSC Ensembl
Innerchr20:62153786..62221249hg19UCSC Ensembl
Innerchr20:61624230..61691693hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3867464
hg1967464
hg1867464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150971
SamplesNINDS_60
Known GenesC20orf195, GMEB2, HELZ2, PTK6, SRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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