A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099967



Internal ID22009200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79607611..79607611hg38UCSC Ensembl
chr13:80181746..80181746hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099967
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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