A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563921



Internal ID21888276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5835468..5835636hg38UCSC Ensembl
chr6:5835701..5835869hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563921
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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