A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005679



Internal ID21915022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53490511..53490704hg38UCSC Ensembl
chr6:53355309..53355502hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005679
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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