A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968762



Internal ID22743697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97182508..97182508hg38UCSC Ensembl
chr14:97648845..97648845hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968762
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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