A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473554



Internal ID21131107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90119031..90173537hg38UCSC Ensembl
chr11:89852199..89906705hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3854507
hg1954507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996396
Samples
Known GenesNAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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