A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401996



Internal ID22459866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36107919..36109270hg38UCSC Ensembl
chr22:36503967..36505318hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381352
hg191352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966517
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401996
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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