A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926926



Internal ID22702154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73614031..73621428hg38UCSC Ensembl
chr10:75373789..75381186hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg387398
hg197398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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