A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061243



Internal ID21970476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101910376..101910376hg38UCSC Ensembl
chr8:102922604..102922604hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588330
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061243
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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