A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098368



Internal ID22007601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110201296..110201296hg38UCSC Ensembl
chr13:110853643..110853643hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610680
Samples
Known GenesCOL4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098368
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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