A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650050



Internal ID21598355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84978037..84978037hg38UCSC Ensembl
chr11:84689081..84689081hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076309
SamplesHG01596
Known GenesDLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650050
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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