A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967098



Internal ID22742033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123449889..123449889hg38UCSC Ensembl
chr8:124462129..124462129hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967098
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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