A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468527



Internal ID21126080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84765007..84782640hg38UCSC Ensembl
chr11:84476050..84493683hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817634
hg1917634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994264
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468527
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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