A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016332



Internal ID78542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125556842..125561713hg38UCSC Ensembl
chr8:126569086..126573957hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg384872
hg194872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016332
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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