A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027009



Internal ID21936352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54811471..54855752hg38UCSC Ensembl
chr15:55103669..55147950hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3844282
hg1944282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027009
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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