A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051286



Internal ID20618326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119874569..119877989hg38UCSC Ensembl
chr1:120417192..120420612hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg383421
hg193421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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