A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685067



Internal ID21206924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36204591..36204881hg38UCSC Ensembl
chr20:34792513..34792803hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802921
Supporting Variants
Samples
Known GenesEPB41L1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685067
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03125


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