A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011599



Internal ID21920942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15594220..15594367hg38UCSC Ensembl
chr6:15594451..15594598hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559268
Samples
Known GenesDTNBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011599
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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