A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205811



Internal ID20772851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105254644..105259083hg38UCSC Ensembl
chr2:105871101..105875540hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg384440
hg194440
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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