A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572308



Internal ID21764351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35425222..35425357hg38UCSC Ensembl
chr6:35392999..35393134hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001615
Supporting Variants
Samples
Known GenesPPARD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572308
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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