A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231079



Internal ID20798119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63455557..63459716hg38UCSC Ensembl
chr6:64165462..64169621hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405291
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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