A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526414



Internal ID20899775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39348363..39349089hg38UCSC Ensembl
chr19:39839003..39839729hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198122
Samples
Known GenesSAMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526414
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer