A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949785



Internal ID16951972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8609674..8619373hg38UCSC Ensembl
Outerchr4:8611401..8621100hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996657
SamplesBILGI_BIOE
Known GenesCPZ
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949785
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