A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586535



Internal ID16027258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63062254..63130372hg38UCSC Ensembl
Innerchr20:61693606..61761724hg19UCSC Ensembl
Innerchr20:61164051..61232169hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3868119
hg1968119
hg1868119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942288
Samples
Known GenesHAR1A, HAR1B, LOC63930
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586535
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