A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022985



Internal ID21932328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37166374..37166428hg38UCSC Ensembl
chr15:37458575..37458629hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022985
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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