A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv631n106



Internal ID19018740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45111212..45111409hg38UCSC Ensembl
chr11:45132763..45132960hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1133260, nsv1130306
SamplesKWS1, KWS2
Known GenesPRDM11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv631n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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