A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525989



Internal ID20899350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10573788..10578864hg38UCSC Ensembl
chr19:10684464..10689540hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385077
hg195077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198034
Samples
Known GenesAP1M2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525989
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