A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567260



Internal ID21759303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142998093..142998334hg38UCSC Ensembl
chr6:143319230..143319471hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019354
Supporting Variants
Samples
Known GenesLOC100507489
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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