A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963875



Internal ID22738811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81350710..81350710hg38UCSC Ensembl
chr8:82262945..82262945hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963875
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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