A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965169



Internal ID22740104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121003206..121003206hg38UCSC Ensembl
chr8:122015446..122015446hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965169
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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