A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438399



Internal ID21095952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27620471..27621189hg38UCSC Ensembl
chr11:27642018..27642736hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989826
Samples
Known GenesBDNF-AS, LINC00678
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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