A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190072



Internal ID20757112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111811278..111812652hg38UCSC Ensembl
chr11:111682002..111683376hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381375
hg191375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461149
Supporting Variants
Samples
Known GenesALG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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