A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989825



Internal ID20556865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27606646..27607157hg38UCSC Ensembl
chr11:27628193..27628704hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451055
Supporting Variants
Samples
Known GenesBDNF-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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