A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv145n106



Internal ID22793973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113484634..113484733hg38UCSC Ensembl
chr1:114027256..114027355hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1137797, nsv1144394
SamplesKWS2, KWS1
Known GenesMAGI3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv145n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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