A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585537



Internal ID21534085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78793791..78796823hg38UCSC Ensembl
chr15:79086133..79089165hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383033
hg193033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086960
SamplesHG03065
Known GenesADAMTS7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585537
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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