A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219004



Internal ID20786044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27615133..27616144hg38UCSC Ensembl
chr11:27636680..27637691hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585603
Supporting Variants
Samples
Known GenesBDNF-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219004
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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