A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657032



Internal ID21605337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9706026..9706026hg38UCSC Ensembl
chr11:9727573..9727573hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076132, nssv17076131
SamplesHG03486, HG00513
Known GenesSWAP70
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657032
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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