A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651630



Internal ID21599935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63893357..63893357hg38UCSC Ensembl
chr11:63660829..63660829hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075623
SamplesHG00731
Known GenesMARK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651630
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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