A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226445



Internal ID20793485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:775945..866869hg38UCSC Ensembl
chr6:775945..866869hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3890925
hg1990925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401810
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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