A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023654



Internal ID21932997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64460702..64460821hg38UCSC Ensembl
chr15:64752901..64753020hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023654
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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