A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089712



Internal ID21432973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65805565..65811310hg38UCSC Ensembl
chr15:66097903..66103648hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385746
hg195746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594636
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089712
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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