A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902473



Internal ID2460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26504826..26513499hg38UCSC Ensembl
chr1:26831317..26839990hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388674
hg198674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902473
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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