A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526006



Internal ID20899367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10784663..10785395hg38UCSC Ensembl
chr18:10784661..10785393hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040240
Samples
Known GenesPIEZO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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