A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453514



Internal ID21111067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15116968..15121159hg38UCSC Ensembl
chr11:15138514..15142705hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384192
hg194192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989368
Samples
Known GenesINSC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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