A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv51n73



Internal ID22782657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39360064..39361380hg38UCSC Ensembl
chr13:39934201..39935517hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv958072, nsv952541
SamplesBILGI_BIOE
Known GenesLHFP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)dgv51n73
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