A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435810



Internal ID21093363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8686227..8689967hg38UCSC Ensembl
chr11:8707774..8711514hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383741
hg193741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994644
Samples
Known GenesRPL27A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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