A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910319



Internal ID22685530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74099318..74099894hg38UCSC Ensembl
chr10:75859076..75859652hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367695
Samples
Known GenesVCL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910319
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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