A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532885



Internal ID20906246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24042920..24046630hg38UCSC Ensembl
chr18:21622884..21626594hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383711
hg193711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040395
Samples
Known GenesTTC39C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532885
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