A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714934



Internal ID138600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79602106..79602785hg38UCSC Ensembl
chr17_gl000204_random:48025..48704hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38680
hg19680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515514
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714934
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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