A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818895



Internal ID21264233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:315875..315875hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13708231, nssv13707003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818895
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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