A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656887



Internal ID21605192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134055477..134055477hg38UCSC Ensembl
chr11:133925372..133925372hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073136
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656887
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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