A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704386



Internal ID15441038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63208233..63221277hg38UCSC Ensembl
Innerchr20:61839585..61852629hg19UCSC Ensembl
Innerchr20:61310030..61323074hg18UCSC Ensembl
Innerchr20:61310030..61323074hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3813045
hg1913045
hg1813045
hg1713045
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527884
Supporting Variants
Samples
Known GenesYTHDF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704386
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