A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216672



Internal ID20783712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154968822..154987899hg38UCSC Ensembl
chr6:155289956..155309033hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3819078
hg1919078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616986
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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