A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864631



Internal ID22639566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13019600..13021349hg38UCSC Ensembl
chr11:13041147..13042896hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864631
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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