A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969355



Internal ID22744290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23657250..23657250hg38UCSC Ensembl
chr15:23902397..23902397hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372571
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969355
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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