A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526102



Internal ID20899463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49020102..49058451hg38UCSC Ensembl
chr19:49523359..49561708hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3838350
hg1938350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198228
Samples
Known GenesCGB, CGB1, CGB2, CGB5, CGB7, CGB8, SNAR-G1, SNAR-G2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526102
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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