A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017495



Internal ID79313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119233936..119237487hg38UCSC Ensembl
chr8:120246176..120249727hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg383552
hg193552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487161
Supporting Variants
Samples
Known GenesMAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017495
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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