A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955023



Internal ID22730245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54468904..54468904hg38UCSC Ensembl
chr8:55381464..55381464hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955023
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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