A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17113255



Internal ID21480857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38755999..38756078hg38UCSC Ensembl
chr2:38983141..38983220hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574165
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17113255
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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