A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587798



Internal ID21536357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78761866..78761917hg38UCSC Ensembl
chr15:79054208..79054259hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080242
SamplesHG03065
Known GenesADAMTS7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587798
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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