A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202414



Internal ID20769454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23517912..23518233hg38UCSC Ensembl
chr1:23844404..23844725hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326630
Supporting Variants
Samples
Known GenesE2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202414
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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