A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016114



Internal ID78389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96455773..96464007hg38UCSC Ensembl
chr8:97468001..97476235hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg388235
hg198235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016114
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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