A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2606n106



Internal ID20161963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134955060..134955724hg38UCSC Ensembl
chr3:134673902..134674566hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112043, nsv1130037, nsv1127112
SamplesKWS1, KWS2
Known GenesEPHB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2606n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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