A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4060n106



Internal ID22797888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68220684..68227984hg38UCSC Ensembl
chr9:70835600..70842900hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg387301
hg197301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115836, nsv1132738
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4060n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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