A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007302



Internal ID21916645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158745098..158753965hg38UCSC Ensembl
chr6:159166130..159174997hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg388868
hg198868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565231
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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