A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523806



Internal ID20897167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46682143..46685286hg38UCSC Ensembl
chr19:47185400..47188543hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg383144
hg193144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046824
Samples
Known GenesPRKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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