A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923719



Internal ID22698946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74029071..74029364hg38UCSC Ensembl
chr10:75788829..75789122hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353841
Samples
Known GenesVCL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923719
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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