A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954102



Internal ID16956289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79739875..79740121hg38UCSC Ensembl
Outerchr18:77499875..77500121hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002758
SamplesBILGI_BIOE
Known GenesCTDP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954102
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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