A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533046



Internal ID20906407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14737233..14986636hg38UCSC Ensembl
chr19:14848045..15097448hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38249404
hg19249404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197412
Samples
Known GenesEMR2, OR7A10, OR7A17, OR7A5, OR7C1, OR7C2, SLC1A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533046
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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