A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1103n106



Internal ID22794931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75054197..75058897hg38UCSC Ensembl
chr14:75520900..75525600hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111921, nsv1120993
SamplesKWS2
Known GenesACYP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1103n106
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