A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442778



Internal ID21100331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20645111..20645668hg38UCSC Ensembl
chr11:20666657..20667214hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989201
Samples
Known GenesSLC6A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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