A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107799



Internal ID21488384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101977790..101978055hg38UCSC Ensembl
chr2:102594252..102594517hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577861
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107799
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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