A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952412



Internal ID17301286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:11958802..11960801hg38UCSC Ensembl
Outerchr18:11958801..11960800hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998845
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952412
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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