A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528919



Internal ID20902280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29269895..29290272hg38UCSC Ensembl
chr19:29760802..29781179hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3820378
hg1920378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047454
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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