A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534466



Internal ID20907827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29520756..29524938hg38UCSC Ensembl
chr19:30011663..30015845hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384183
hg194183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047477
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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