A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949812



Internal ID17298686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:119402846..119410345hg38UCSC Ensembl
Outerchr4:120324001..120331500hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996772
SamplesBILGI_BIOE
Known GenesLINC01061
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949812
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