A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909131



Internal ID22684341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103080185..103081488hg38UCSC Ensembl
chr8:104092413..104093716hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909131
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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