A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910015



Internal ID22685225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94861802..94862192hg38UCSC Ensembl
chr8:95874030..95874420hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443348
Samples
Known GenesINTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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