A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919231



Internal ID22694453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98054986..98063919hg38UCSC Ensembl
chr8:99067214..99076147hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg388934
hg198934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919231
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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