A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2788852



Internal ID21234190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17709964..17709964hg38UCSC Ensembl
chr10:17751963..17751963hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13679519
Samples
Known GenesSTAM
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2788852
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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