A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524255



Internal ID20897616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56402101..56407200hg38UCSC Ensembl
chr19:56913470..56918569hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199678
Samples
Known GenesZNF583
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524255
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