A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324484



Internal ID20857611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16238696..16267374hg38UCSC Ensembl
chr1:16565191..16593869hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3828679
hg1928679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201893
Samples
Known GenesFBXO42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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