A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523076



Internal ID20896437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19607126..19609974hg38UCSC Ensembl
chr19:19717935..19720783hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382849
hg192849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045441
Samples
Known GenesPBX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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