A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528656



Internal ID20902017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10455142..10455390hg38UCSC Ensembl
chr19:10565818..10566066hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044305
Samples
Known GenesPDE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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