A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519510



Internal ID20892871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34403322..34417336hg38UCSC Ensembl
chr19:34894227..34908241hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3814015
hg1914015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046228
Samples
Known GenesPDCD2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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