A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1750n106



Internal ID22795578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27240892..27250792hg38UCSC Ensembl
chr19:27731800..27741700hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg389901
hg199901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1128780, nsv1124782
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1750n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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