A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054562



Internal ID21963795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9132126..9132126hg38UCSC Ensembl
chr2:9272255..9272255hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382379
hg192379
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054562
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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