A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263093



Internal ID20472311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27523985..27524267hg38UCSC Ensembl
chr11:27545532..27545814hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742338
Supporting Variants
Samples
Known GenesBDNF-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263093
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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