A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527333



Internal ID20900694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49321678..49336517hg38UCSC Ensembl
chr19:49824935..49839774hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3814840
hg1914840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198243
Samples
Known GenesCD37, SLC6A16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527333
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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