A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022844



Internal ID21932187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57308084..57308144hg38UCSC Ensembl
chr15:57600282..57600342hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022844
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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