A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663628



Internal ID21611933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3150126..3150126hg38UCSC Ensembl
chr11:3171356..3171356hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073955
SamplesNA19650
Known GenesOSBPL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663628
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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