A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923512



Internal ID22698739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98044322..98044572hg38UCSC Ensembl
chr10:99804079..99804329hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923512
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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