A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569956



Internal ID21761999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116088891..116088891hg38UCSC Ensembl
chr6:116410054..116410054hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569956
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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