A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198809



Internal ID20765849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41345657..41368887hg38UCSC Ensembl
chr19:41851562..41874792hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823231
hg1923231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517594
Supporting Variants
Samples
Known GenesB9D2, TGFB1, TMEM91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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