A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021937



Internal ID21931280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48662187..48662828hg38UCSC Ensembl
chr15:48954384..48955025hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021937
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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