A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440893



Internal ID21098446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2897100..2902889hg38UCSC Ensembl
chr11:2918330..2924119hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385790
hg195790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990426
Samples
Known GenesSLC22A18, SLC22A18AS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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