A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963747



Internal ID22738682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15178372..15178372hg38UCSC Ensembl
chr10:15220371..15220371hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963747
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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