A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3411n106



Internal ID22797239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149314944..149315357hg38UCSC Ensembl
chr6:149636080..149636493hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112141, nsv1111707
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3411n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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