A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696265



Internal ID21218119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39101646..39101707hg38UCSC Ensembl
chr22:39497651..39497712hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804639
Supporting Variants
Samples
Known GenesAPOBEC3H
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.833333


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