A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521817



Internal ID20895178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24429989..24431542hg38UCSC Ensembl
chr18:22009953..22011506hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039477
Samples
Known GenesIMPACT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521817
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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