A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925078



Internal ID22700305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102087102..102092459hg38UCSC Ensembl
chr10:103846859..103852216hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385358
hg195358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925078
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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