A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112759



Internal ID21463417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25953614..25953920hg38UCSC Ensembl
chr2:26176483..26176789hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566892
Supporting Variants
SamplesHG03009
Known GenesKIF3C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112759
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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