A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179899



Internal ID20746939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29598401..29602700hg38UCSC Ensembl
chr11:29619948..29624247hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454017
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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