A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523221



Internal ID21847580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10806477..10806477hg38UCSC Ensembl
chr2:10946603..10946603hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382783
hg192783
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056144
Supporting Variants
Samples
Known GenesPDIA6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523221
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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