A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110867



Internal ID21505358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18854471..18854522hg38UCSC Ensembl
chr2:19035737..19035788hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578490
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110867
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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