A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062970



Internal ID21972203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121936133..121936133hg38UCSC Ensembl
chr8:122948372..122948372hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062970
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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