A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974042



Internal ID22748977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95415149..95415149hg38UCSC Ensembl
chr13:96067403..96067403hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974042
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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