A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2353n106



Internal ID20161710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10419904..10422695hg38UCSC Ensembl
chr21:11089762..11092553hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg382792
hg192792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135574, nsv1130019, nsv1126983
SamplesKWS2, KWS1
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2353n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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