A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099159



Internal ID21409727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54626444..54626752hg38UCSC Ensembl
chr16:54660356..54660664hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592281
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099159
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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