A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973924



Internal ID22748859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78227631..78227631hg38UCSC Ensembl
chr11:77938677..77938677hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365428
Samples
Known GenesGAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973924
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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