A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098095



Internal ID22007328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61310729..61310729hg38UCSC Ensembl
chr13:61884862..61884862hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098095
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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