A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525082



Internal ID21849440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26973681..26973681hg38UCSC Ensembl
chr2:27196549..27196549hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042836
Supporting Variants
Samples
Known GenesMAPRE3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525082
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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