A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1433n106



Internal ID22795261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21290388..21351688hg38UCSC Ensembl
chr17:21193700..21255000hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3861301
hg1961301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110294, nsv1141303
SamplesKWS2, KWS1
Known GenesMAP2K3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1433n106
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