A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908372



Internal ID6373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93830684..93837025hg38UCSC Ensembl
chr1:94296240..94302581hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg386342
hg196342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430434
Supporting Variants
Samples
Known GenesBCAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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