A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534999



Internal ID310716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91384463..91384495hg38UCSC Ensembl
chr10:93144220..93144252hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036894
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534999
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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