A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202121



Internal ID20769161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97300425..97333016hg38UCSC Ensembl
chr1:97765981..97798572hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3832592
hg1932592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323399
Supporting Variants
Samples
Known GenesDPYD, DPYD-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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