A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097547



Internal ID22006780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26075628..26075628hg38UCSC Ensembl
chr16:26086949..26086949hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620330
Samples
Known GenesHS3ST4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097547
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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