A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943825



Internal ID16237781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63608014..63620691hg38UCSC Ensembl
Innerchr20:62239367..62252044hg19UCSC Ensembl
Innerchr20:61709811..61722488hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3812678
hg1912678
hg1812678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586605
Supporting Variants
Samples
Known GenesGMEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943825
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