A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562639



Internal ID21886994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89052070..89055391hg38UCSC Ensembl
chr6:89761789..89765110hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383322
hg193322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016652
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562639
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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