A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087659



Internal ID21996892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44277449..44277449hg38UCSC Ensembl
chr13:44851585..44851585hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087659
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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