A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076132



Internal ID21412182
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 StatusS
Merged Variantsnsv5657032
Supporting Variants
SamplesHG00513
Known GenesSWAP70
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076132
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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