A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526217



Internal ID21850575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7259303..7259389hg38UCSC Ensembl
chr2:7399434..7399520hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526217
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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