A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949783



Internal ID16951970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8044374..8066473hg38UCSC Ensembl
Outerchr4:8046101..8068200hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3822100
hg1922100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996655
SamplesBILGI_BIOE
Known GenesABLIM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949783
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