A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908348



Internal ID6360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93367690..93373359hg38UCSC Ensembl
chr1:93833247..93838916hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg385670
hg195670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908348
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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