A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052848



Internal ID20619888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165856329..165857310hg38UCSC Ensembl
chr1:165825566..165826547hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38982
hg19982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323521
Supporting Variants
Samples
Known GenesUCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00014


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