A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804639



Internal ID21249977
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 StatusM
Merged Variants
Supporting Variantsnssv13696265
Samples
Known GenesAPOBEC3H
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804639
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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