A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468612



Internal ID21126165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90139964..90140404hg38UCSC Ensembl
chr11:89873132..89873572hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996400
Samples
Known GenesNAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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