A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524988



Internal ID20898349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11855906..11857123hg38UCSC Ensembl
chr18:11855905..11857122hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381218
hg191218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038739
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer