A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4061n106



Internal ID22797889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68293984..68297084hg38UCSC Ensembl
chr9:70908900..70912000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg383101
hg193101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115838, nsv1129052
SamplesKWS2, KWS1
Known GenesCBWD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4061n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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