A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563896



Internal ID7034996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:45951002..45957693hg38UCSC Ensembl
Outerchr20:44579641..44586332hg19UCSC Ensembl
Outerchr20:44013048..44019739hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386692
hg196692
hg186692
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000107
Supporting Variants
SamplesHuRef
Known GenesZNF335
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563896
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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