A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525061



Internal ID21849419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43512242..43515404hg38UCSC Ensembl
chr2:43739381..43742543hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg383163
hg193163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989176
Supporting Variants
Samples
Known GenesTHADA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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