A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036096



Internal ID21945439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79840183..79840239hg38UCSC Ensembl
chr15:80132525..80132581hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036096
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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