A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699100



Internal ID21220948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58542196..58542339hg38UCSC Ensembl
chr20:57117252..57117395hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802920
Supporting Variants
Samples
Known GenesAPCDD1L-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699100
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.95


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