A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333840



Internal ID20867021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179255381..179275672hg38UCSC Ensembl
chr1:179224516..179244807hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3820292
hg1920292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333840
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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