A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661870



Internal ID21610175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67222609..67222609hg38UCSC Ensembl
chr11:66990080..66990080hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075308
SamplesHG00731
Known GenesKDM2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661870
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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