A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221486



Internal ID20788526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30289908..30322966hg38UCSC Ensembl
chr6:30257685..30290743hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3833059
hg1933059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397160
Supporting Variants
Samples
Known GenesHCG17, HCG18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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