A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086696



Internal ID21451154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52104739..52107648hg38UCSC Ensembl
chr15:52396936..52399845hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382910
hg192910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598621
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086696
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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