A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521607



Internal ID20894968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45581991..45583367hg38UCSC Ensembl
chr19:46085249..46086625hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381377
hg191377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046510
Samples
Known GenesOPA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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