A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526916



Internal ID21851273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11356628..11376564hg38UCSC Ensembl
chr2:11496754..11516690hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3819937
hg1919937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526916
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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