A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968500



Internal ID22743435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40374556..40374556hg38UCSC Ensembl
chr15:40666757..40666757hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968500
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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