A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049724



Internal ID21958957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128409570..128409570hg38UCSC Ensembl
chr2:129167144..129167144hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049724
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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