A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482987



Internal ID260430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:76484548..76484775hg38UCSC Ensembl
chr8:77396783..77397010hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012231
Samples
Known GenesLINC01111
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482987
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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