A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681599



Internal ID15071565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63562092..63581575hg38UCSC Ensembl
Innerchr20:62193445..62212928hg19UCSC Ensembl
Innerchr20:61663889..61683372hg18UCSC Ensembl
Innerchr20:61663889..61683372hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3819484
hg1919484
hg1819484
hg1719484
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517702
Supporting Variants
Samples
Known GenesHELZ2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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