A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2553n106



Internal ID22796381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81858341..81858681hg38UCSC Ensembl
chr3:81907492..81907832hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135590, nsv1135143, nsv1145392
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2553n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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