A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081255



Internal ID21444715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83105121..83105449hg38UCSC Ensembl
chr15:83773873..83774201hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589269
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081255
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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