A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523620



Internal ID20896981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37609360..37681915hg38UCSC Ensembl
chr19:38100261..38172816hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3872556
hg1972556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198085
Samples
Known GenesZFP30, ZNF540, ZNF781
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523620
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