A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530021



Internal ID20903382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36007849..36020429hg38UCSC Ensembl
chr19:36498751..36511331hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812581
hg1912581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197795
Samples
Known GenesALKBH6, CLIP3, SYNE4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530021
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