A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574118



Internal ID21766161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108270239..108270367hg38UCSC Ensembl
chr6:108591443..108591571hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574118
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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