A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012000



Internal ID75667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69978575..69980290hg38UCSC Ensembl
chr8:70890810..70892525hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg381716
hg191716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012000
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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