A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904773



Internal ID4001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38967341..38975311hg38UCSC Ensembl
chr1:39433013..39440983hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387971
hg197971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904773
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002811


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