A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904253



Internal ID3654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71319127..71389858hg38UCSC Ensembl
chr1:71784810..71855541hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3870732
hg1970732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904253
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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