A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199767



Internal ID20766807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118825072..118847585hg38UCSC Ensembl
chr1:119367695..119390208hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3822514
hg1922514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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