A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523234



Internal ID21847593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2762301..2762372hg38UCSC Ensembl
chr2:2766073..2766144hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523234
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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