A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525872



Internal ID20899233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46294647..46314823hg38UCSC Ensembl
chr19:46797904..46818080hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3820177
hg1920177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046790
Samples
Known GenesHIF3A, RNU6-66P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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