A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521629



Internal ID21845988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25448642..25448729hg38UCSC Ensembl
chr2:25671511..25671598hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988621
Supporting Variants
Samples
Known GenesDTNB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521629
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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