A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558838



Internal ID21883193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116299515..116299567hg38UCSC Ensembl
chr6:116620678..116620730hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017595
Supporting Variants
Samples
Known GenesDSE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558838
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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