A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126636



Internal ID21417566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39101634..39101695hg38UCSC Ensembl
chr22:39497639..39497700hg19UCSC 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 Variantsnsv5588581
Supporting Variants
SamplesHG00731
Known GenesAPOBEC3H
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126636
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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