A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033923



Internal ID21943266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75414391..75415585hg38UCSC Ensembl
chr11:75125435..75126629hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592888
Samples
Known GenesRPS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033923
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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