A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041076



Internal ID21950412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155781612..155781612hg38UCSC Ensembl
chr2:156638124..156638124hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041076
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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