A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529065



Internal ID21853422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:115538612..115538612hg38UCSC Ensembl
chr2:116296188..116296188hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049092
Supporting Variants
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529065
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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