A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv518n106



Internal ID20159875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112949441..112951941hg38UCSC Ensembl
chr10:114709200..114711700hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121821, nsv1143648
SamplesKWS2, KWS1
Known GenesTCF7L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv518n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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