A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945092



Internal ID21365161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39101634..39101696hg38UCSC Ensembl
chr22:39497639..39497701hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179507
SamplesHG002
Known GenesAPOBEC3H
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945092
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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