A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991826



Internal ID61982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3796836..3816840hg38UCSC Ensembl
chr7:3836468..3856472hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3820005
hg1920005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463600
Supporting Variants
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991826
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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