A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333535



Internal ID20866713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65066501..65068900hg38UCSC Ensembl
chr1:65532184..65534583hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333535
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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