A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526497



Internal ID20899858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15219271..15233990hg38UCSC Ensembl
chr19:15330082..15344801hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3814720
hg1914720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197419
Samples
Known GenesEPHX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526497
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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