A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv519n106



Internal ID22794347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115952089..115952491hg38UCSC Ensembl
chr10:117711600..117712002hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1132236, nsv1111373, nsv1128271
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv519n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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