A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848539



Internal ID22623474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3383591..3386690hg38UCSC Ensembl
chr11:3404821..3407920hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457866
Samples
Known GenesLOC650368
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848539
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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