A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097895



Internal ID22007128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30323506..30323506hg38UCSC Ensembl
chr13:30897643..30897643hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097895
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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