A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517011



Internal ID20890372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4160675..4164017hg38UCSC Ensembl
chr19:4160672..4164014hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383343
hg193343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046360
Samples
Known GenesCREB3L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517011
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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