A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1196n106



Internal ID20160553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41561637..41562558hg38UCSC Ensembl
chr15:41853835..41854756hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38922
hg19922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1134435, nsv1143322
SamplesKWS2, KWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1196n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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