A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9n106



Internal ID22793837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1207339..1207760hg38UCSC Ensembl
chr1:1142719..1143140hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1134959, nsv1121063
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv9n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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