A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857150



Internal ID22632085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118726948..118728731hg38UCSC Ensembl
chr11:118597657..118599440hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452585, nssv17461145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857150
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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