A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089593



Internal ID21407038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58993694..58994110hg38UCSC Ensembl
chr16:59027598..59028014hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590300
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089593
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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