A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449356



Internal ID21106909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22365630..22366080hg38UCSC Ensembl
chr11:22387176..22387626hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989549
Samples
Known GenesSLC17A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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