A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528606



Internal ID20901967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34423459..34423765hg38UCSC Ensembl
chr19:34914364..34914670hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046230
Samples
Known GenesPDCD2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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