A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1928n106



Internal ID22795756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66762911..66762999hg38UCSC Ensembl
chr2:66990043..66990131hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119477, nsv1141792
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1928n106
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