A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086318



Internal ID21995551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111340803..111340803hg38UCSC Ensembl
chr13:111993150..111993150hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605957
Samples
Known GenesTEX29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086318
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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