A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546919



Internal ID320818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1435449..1435462hg38UCSC Ensembl
chr10:1477644..1477657hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030973
Samples
Known GenesADARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546919
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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