A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978529



Internal ID22753464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110796884..110796884hg38UCSC Ensembl
chr13:111449231..111449231hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978529
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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