A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv453n106



Internal ID19018562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48709111..48709434hg38UCSC Ensembl
chr10:49917156..49917479hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1116983, nsv1137920
SamplesKWS1, KWS2
Known GenesWDFY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv453n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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