A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158675



Internal ID21475689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8842098..8842148hg38UCSC Ensembl
chr5:8842210..8842260hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568798
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158675
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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