A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1569n106



Internal ID22795397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26991656..26992427hg38UCSC Ensembl
chr18:24571620..24572391hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111955, nsv1135051
SamplesKWS2, KWS1
Known GenesCHST9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1569n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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