A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1710n106



Internal ID19019819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9900824..9901424hg38UCSC Ensembl
chr19:10011500..10012100hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1144863, nsv1121968
SamplesKWS1, KWS2
Known GenesOLFM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1710n106
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