A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596056



Internal ID21544663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75336345..75336513hg38UCSC Ensembl
chr15:75628686..75628854hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094528
SamplesHG03065
Known GenesCOMMD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596056
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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