A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849952



Internal ID22624887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38345388..38366520hg38UCSC Ensembl
chr11:38366938..38388070hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3821133
hg1921133
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849952
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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