A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049202



Internal ID21958437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149748028..149748028hg38UCSC Ensembl
chr2:150604542..150604542hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049202
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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