A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050543



Internal ID21959776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101899525..101899525hg38UCSC Ensembl
chr2:102515987..102515987hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg385966
hg195966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050543
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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