A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018445



Internal ID21927788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27190743..27192106hg38UCSC Ensembl
chr6:27158522..27159885hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018445
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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