A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086675



Internal ID21995908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30673633..30673633hg38UCSC Ensembl
chr13:31247770..31247770hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086675
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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