A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052628



Internal ID20619668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163760834..163920861hg38UCSC Ensembl
chr1:163730071..163890098hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38160028
hg19160028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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