A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464511



Internal ID21122064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84613915..84655711hg38UCSC Ensembl
chr11:84324958..84366754hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3841797
hg1941797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994901
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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