A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329569



Internal ID20862721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171219363..171224390hg38UCSC Ensembl
chr1:171188502..171193529hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg385028
hg195028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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