A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923715



Internal ID22698942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22372432..22376858hg38UCSC Ensembl
chr10:22661361..22665787hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384427
hg194427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364808
Samples
Known GenesSPAG6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923715
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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