A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924484



Internal ID22699711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102805626..102805933hg38UCSC Ensembl
chr10:104565383..104565690hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359051
Samples
Known GenesWBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924484
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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