A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135464



Internal ID20702425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11240097..11241410hg38UCSC Ensembl
chr6:11240330..11241643hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg381314
hg191314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404915
Supporting Variants
Samples
Known GenesNEDD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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