A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109386



Internal ID21504133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156220599..156220821hg38UCSC Ensembl
chr2:157077111..157077333hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575652
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109386
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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