A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334970



Internal ID20868160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241357601..241361800hg38UCSC Ensembl
chr1:241520901..241525100hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334970
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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