A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112754



Internal ID21489547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25634224..25634334hg38UCSC Ensembl
chr2:25857093..25857203hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578304
Supporting Variants
SamplesNA18939
Known GenesDTNB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112754
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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