A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191708



Internal ID20758748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68967083..68987217hg38UCSC Ensembl
chr11:68734552..68754685hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3820135
hg1920134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474873
Supporting Variants
Samples
Known GenesMRGPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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