A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968432



Internal ID22743367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70430598..70430598hg38UCSC Ensembl
chr14:70897315..70897315hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968432
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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