A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656993



Internal ID21605298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130888727..130888727hg38UCSC Ensembl
chr11:130758622..130758622hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073541
SamplesNA19239
Known GenesSNX19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656993
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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