A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054163



Internal ID21963396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160174769..160174769hg38UCSC Ensembl
chr2:161031280..161031280hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522635
Samples
Known GenesITGB6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054163
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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