A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481676



Internal ID259145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1326000..1422000hg38UCSC Ensembl
chr10:1368195..1464195hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3896001
hg1996001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030959
Samples
Known GenesADARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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