A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090228



Internal ID21440170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81669285..81669375hg38UCSC Ensembl
chr16:81702890..81702980hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602397
Supporting Variants
SamplesHG00732
Known GenesCMIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090228
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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