A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259125



Internal ID20468313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132600791..132600791hg38UCSC Ensembl
chr6:132921930..132921930hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259125
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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