A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026891



Internal ID21936234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15116834..15116900hg38UCSC Ensembl
chr11:15138380..15138446hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587244
Samples
Known GenesINSC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026891
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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