A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397728



Internal ID22455598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35439075..35439466hg38UCSC Ensembl
chr22:35835068..35835459hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397728
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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