A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2622n106



Internal ID20161979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155025783..155025852hg38UCSC Ensembl
chr3:154743572..154743641hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1131741, nsv1139171
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2622n106
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