A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2269n106



Internal ID22796097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56365902..56366005hg38UCSC Ensembl
chr20:54940958..54941061hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119634, nsv1136555
SamplesKWS2, KWS1
Known GenesFAM210B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2269n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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