A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020408



Internal ID21929751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157338449..157343265hg38UCSC Ensembl
chr7:157131143..157135959hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384817
hg194817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577308
Samples
Known GenesDNAJB6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020408
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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