A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233103



Internal ID20800143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6878426..6894997hg38UCSC Ensembl
chr6:6878659..6895230hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3816572
hg1916572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233103
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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