A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv369n106



Internal ID20159726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18214146..18214679hg38UCSC Ensembl
chr10:18503075..18503608hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111442, nsv1135409, nsv1127600
SamplesKWS1, KWS2
Known GenesCACNB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv369n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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