A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975232



Internal ID22750167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77646734..77646734hg38UCSC Ensembl
chr11:77357779..77357779hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975232
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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