A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653797



Internal ID15043763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45945599..45965589hg38UCSC Ensembl
Innerchr20:44574238..44594228hg19UCSC Ensembl
Innerchr20:44007645..44027635hg18UCSC Ensembl
Innerchr20:44007645..44027635hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3819991
hg1919991
hg1819991
hg1719991
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517296
Supporting Variants
Samples
Known GenesPCIF1, ZNF335
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653797
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