A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952418



Internal ID17301292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14854702..14871401hg38UCSC Ensembl
Outerchr18:14854701..14871400hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3816700
hg1916700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998851
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952418
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer