A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226898



Internal ID20793938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7426813..7457347hg38UCSC Ensembl
chr6:7427046..7457580hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3830535
hg1930535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00097


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