A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012733



Internal ID76159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57307065..57310404hg38UCSC Ensembl
chr8:58219624..58222963hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg383340
hg193340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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