A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205760



Internal ID20772800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100561355..100576007hg38UCSC Ensembl
chr2:101177817..101192469hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3814653
hg1914653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344266
Supporting Variants
Samples
Known GenesPDCL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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