A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223763



Internal ID20790803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78136801..78339500hg38UCSC Ensembl
chr6:78846518..79049217hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38202700
hg19202700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0005


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