A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185173



Internal ID20752213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119122922..119126152hg38UCSC Ensembl
chr11:118993632..118996862hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383231
hg193231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472530
Supporting Variants
Samples
Known GenesHINFP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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