A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216929



Internal ID20783969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144114474..144135051hg38UCSC Ensembl
chr6:144435611..144456188hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3820578
hg1920578
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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