A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567873



Internal ID21759916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35384463..35385038hg38UCSC Ensembl
chr6:35352240..35352815hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015774
Supporting Variants
Samples
Known GenesPPARD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567873
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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