A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905219



Internal ID4291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79320517..79349391hg38UCSC Ensembl
chr1:79786202..79815076hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3828875
hg1928875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905219
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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