A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529545



Internal ID20902906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48622514..48797442hg38UCSC Ensembl
chr19:49125771..49300699hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38174929
hg19174929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199593
Samples
Known GenesBCAT2, CA11, DBP, FGF21, FUT1, FUT2, IZUMO1, MAMSTR, NTN5, RASIP1, SEC1P, SPHK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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