A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212063



Internal ID20779103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149844819..149916579hg38UCSC Ensembl
chr4:150765971..150837731hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3871761
hg1971761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212063
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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