A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798127



Internal ID21243465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59233685..59233685hg38UCSC Ensembl
chr18:56900917..56900917hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13686063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798127
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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