A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063508



Internal ID21972741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63477537..63477537hg38UCSC Ensembl
chr8:64390095..64390095hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063508
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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