A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661739



Internal ID21610044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62951867..62951867hg38UCSC Ensembl
chr11:62719339..62719339hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075594
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661739
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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