A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904895



Internal ID4080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44997585..44998247hg38UCSC Ensembl
chr1:45463257..45463919hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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