A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491842



Internal ID269069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142196282..142337354hg38UCSC Ensembl
chr8:143277643..143418715hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38141073
hg19141073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019272
Samples
Known GenesLINC00051, TSNARE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491842
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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