A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952239



Internal ID17301113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:100165764..100168663hg38UCSC Ensembl
Outerchr14:100632101..100635000hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998399
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952239
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