A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3399n106



Internal ID20162756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136268339..136269473hg38UCSC Ensembl
chr6:136589477..136590611hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1109370, nsv1130111, nsv1112136
SamplesKWS2, KWS1
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3399n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer