A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4010n106



Internal ID22797838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42662197..42670897hg38UCSC Ensembl
chr9:44339000..44347700hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388701
hg198701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1141612, nsv1129010
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4010n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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