A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv131n73



Internal ID22782737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184159013..184159612hg38UCSC Ensembl
chr3:183876801..183877400hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv955529, nsv950018
SamplesBILGI_BIOE
Known GenesDVL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)dgv131n73
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