A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564362



Internal ID21888717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19939745..19939848hg38UCSC Ensembl
chr6:19939976..19940079hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013577
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564362
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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