A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056547



Internal ID20623587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199626872..199749406hg38UCSC Ensembl
chr1:199596000..199718534hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38122535
hg19122535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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