A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903626



Internal ID3234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32471713..32471763hg38UCSC Ensembl
chr1:32937314..32937364hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430742
Supporting Variants
Samples
Known GenesZBTB8B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903626
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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