A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860312



Internal ID22635247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81554325..81569336hg38UCSC Ensembl
chr11:81265367..81280378hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3815012
hg1915012
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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