A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952860



Internal ID16955047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:69053584..69055983hg38UCSC Ensembl
Outerchr14:69520301..69522700hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998363
SamplesBILGI_BIOE
Known GenesDCAF5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952860
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