A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519543



Internal ID20892904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39145435..39146274hg38UCSC Ensembl
chr19:39636075..39636914hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047860
Samples
Known GenesPAK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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