A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322473



Internal ID20855586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:191922158..191946789hg38UCSC Ensembl
chr1:191891288..191915919hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3824632
hg1924632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322473
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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