A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904771



Internal ID4000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38952245..38960086hg38UCSC Ensembl
chr1:39417917..39425758hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387842
hg197842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430159
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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