A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526106



Internal ID20899467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39396213..39396847hg38UCSC Ensembl
chr19:39886853..39887487hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047876
Samples
Known GenesMED29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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