A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325613



Internal ID20858744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:97853343..97857613hg38UCSC Ensembl
chr1:98318899..98323169hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg384271
hg194271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065750
Samples
Known GenesDPYD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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