A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976639



Internal ID22751574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77430380..77430380hg38UCSC Ensembl
chr13:78004515..78004515hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976639
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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