A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv449n106



Internal ID20159806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47437562..47461362hg38UCSC Ensembl
chr10:48278000..48301800hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3823801
hg1923801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112586, nsv1118174
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv449n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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