A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518736



Internal ID20892097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33003382..33005412hg38UCSC Ensembl
chr19:33494288..33496318hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382031
hg192031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047695
Samples
Known GenesRHPN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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