A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528387



Internal ID20901748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22198462..22213440hg38UCSC Ensembl
chr18:19778424..19793403hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3814979
hg1914980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179014
Samples
Known GenesGATA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528387
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