A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118463



Internal ID21487612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26152534..26152534hg38UCSC Ensembl
chr21:27524852..27524852hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668800
Supporting Variants
SamplesNA18534
Known GenesAPP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118463
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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