A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450281



Internal ID21107834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18573781..18574977hg38UCSC Ensembl
chr11:18595328..18596524hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988656
Samples
Known GenesUEVLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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