A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015774



Internal ID21925117
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 StatusM
Merged Variants
Supporting Variantsnssv17567873
Samples
Known GenesPPARD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015774
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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