A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890343



Internal ID167726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9583197..9583974hg38UCSC Ensembl
chr1:9643255..9644032hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420676
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890343
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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