A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663657



Internal ID21611962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68207790..68207790hg38UCSC Ensembl
chr11:67975257..67975257hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382416
hg192416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075475, nssv17075476
SamplesHG00096, NA12329
Known GenesSUV420H1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663657
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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