A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv382n106



Internal ID20159739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26710071..26713271hg38UCSC Ensembl
chr10:26999000..27002200hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1143496, nsv1130645
SamplesKWS1, KWS2
Known GenesPDSS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv382n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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