A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17019782



Internal ID80827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135256222..135269000hg38UCSC Ensembl
chr8:136268465..136281243hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3812779
hg1912779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142086
Supporting Variants
Samples
Known GenesLOC286094
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17019782
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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