A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317759



Internal ID20850848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97421444..97421975hg38UCSC Ensembl
chr1:97887000..97887531hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065682
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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