A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097597



Internal ID21482477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41031557..41031611hg38UCSC Ensembl
chr15:41323755..41323809hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588030
Supporting Variants
SamplesHG03732
Known GenesINO80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097597
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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