A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316599



Internal ID20849679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16321325..16379819hg38UCSC Ensembl
chr1:16647820..16706314hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3858495
hg1958495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201903
Samples
Known GenesFBXO42, SZRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316599
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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