A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656157



Internal ID21604462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3204210..3204210hg38UCSC Ensembl
chr11:3225440..3225440hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073967
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656157
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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