A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092940



Internal ID21431720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81085859..81086211hg38UCSC Ensembl
chr16:81119464..81119816hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588285
Supporting Variants
SamplesHG00731
Known GenesGCSH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092940
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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