A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086099



Internal ID21467009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35656602..35656727hg38UCSC Ensembl
chr15:35948803..35948928hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588270
Supporting Variants
SamplesHG03065
Known GenesDPH6-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086099
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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