A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091158



Internal ID21408964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79840183..79840238hg38UCSC Ensembl
chr15:80132525..80132580hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604000
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091158
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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