A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857261



Internal ID22632196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96587975..96591689hg38UCSC Ensembl
chr11:96458975..96462689hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383715
hg193715
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857261
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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