A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563892



Internal ID336818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86443264..86443299hg38UCSC Ensembl
chr10:88203021..88203056hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038324
Samples
Known GenesWAPAL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563892
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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