A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927463



Internal ID22702691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81275717..81276558hg38UCSC Ensembl
chr8:82187952..82188793hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927463
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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