A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074694



Internal ID21446119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44663739..44663739hg38UCSC Ensembl
chr11:44685289..44685289hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658993
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074694
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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