A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899847



Internal ID679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17191097..17191385hg38UCSC Ensembl
chr1:17517592..17517880hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899847
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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