A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096588



Internal ID21405295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85451553..85451634hg38UCSC Ensembl
chr16:85485159..85485240hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591151
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096588
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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