A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867016



Internal ID22641951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119031487..119034427hg38UCSC Ensembl
chr11:118902197..118905137hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382941
hg192941
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv290n209
Supporting Variantsnssv17458586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867016
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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