A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516486



Internal ID20889847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11066887..11081986hg38UCSC Ensembl
chr18:11066886..11081985hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3815100
hg1915100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038671
Samples
Known GenesPIEZO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516486
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