A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006112



Internal ID21915455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158049855..158049929hg38UCSC Ensembl
chr6:158470887..158470961hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563660
Samples
Known GenesSYNJ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006112
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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