A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018019



Internal ID21927362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70235010..70235947hg38UCSC Ensembl
chr6:70944713..70945650hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570197
Samples
Known GenesCOL9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018019
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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