A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073452



Internal ID21437655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124586226..124586226hg38UCSC Ensembl
chr11:124456122..124456122hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650008
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073452
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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