A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908336



Internal ID6353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93261204..93261388hg38UCSC Ensembl
chr1:93726761..93726945hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417741
Supporting Variants
Samples
Known GenesCCDC18
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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