A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv161n106



Internal ID22793989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121742140..121742197hg38UCSC Ensembl
chr1:121483938..121483995hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1127025, nsv1133897
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv161n106
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