A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063172



Internal ID21972405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62217183..62217183hg38UCSC Ensembl
chr8:63129742..63129742hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063172
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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