A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054147



Internal ID21963380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230913805..230913805hg38UCSC Ensembl
chr2:231778520..231778520hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg383064
hg193064
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533233
Samples
Known GenesGPR55
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054147
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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