A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031813



Internal ID21941156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75055277..75055350hg38UCSC Ensembl
chr15:75347618..75347691hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031813
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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