A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559368



Internal ID21883723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42753976..42754035hg38UCSC Ensembl
chr6:42721714..42721773hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018560
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559368
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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