A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155271



Internal ID21465396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135946933..135947176hg38UCSC Ensembl
chr8:136959176..136959419hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580703
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155271
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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