A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886825



Internal ID22661814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17039195..17039246hg38UCSC Ensembl
chr1:17365690..17365741hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363747
Samples
Known GenesSDHB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886825
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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