A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4026n106



Internal ID22797854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62799268..62799394hg38UCSC Ensembl
chr9:66455092..66455218hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110017, nsv1140976
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4026n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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