A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455623



Internal ID21113176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118214427..118215908hg38UCSC Ensembl
chr11:118085142..118086623hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381482
hg191482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987184
Samples
Known GenesAMICA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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