A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4124n106



Internal ID22797952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109667920..109668332hg38UCSC Ensembl
chr9:112430200..112430612hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135295, nsv1112200, nsv1109895
SamplesKWS2, KWS1
Known GenesPALM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4124n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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