A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2788190



Internal ID21233528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103251101..103251101hg38UCSC Ensembl
chr10:105010858..105010858hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2788190
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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