A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17108609



Internal ID21425679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143801119..143801270hg38UCSC Ensembl
chr2:144558688..144558839hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584300
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17108609
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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