A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332431



Internal ID20865602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115561101..115569600hg38UCSC Ensembl
chr1:116103722..116112221hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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