A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437996



Internal ID22495866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22049287..22053475hg38UCSC Ensembl
chr6:22049516..22053704hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384189
hg194189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898415
Supporting Variants
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437996
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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