A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849337



Internal ID22624272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62355860..62358971hg38UCSC Ensembl
chr11:62123332..62126443hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg383112
hg193112
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459391
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849337
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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