A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036224



Internal ID21945567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26233031..26238981hg38UCSC Ensembl
chr15:26478178..26484128hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385951
hg195951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036224
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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