A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015192



Internal ID21924535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75525127..75529190hg38UCSC Ensembl
chr6:76234843..76238906hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384064
hg194064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015192
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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