A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452474



Internal ID21110027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3915529..3924300hg38UCSC Ensembl
chr11:3936759..3945530hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388772
hg198772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990773
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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