A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520765



Internal ID21845124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112732378..112732378hg38UCSC Ensembl
chr2:113489955..113489955hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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