A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328627



Internal ID20861775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235697447..235698476hg38UCSC Ensembl
chr1:235860747..235861776hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058882
Samples
Known GenesLYST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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