A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1614n106



Internal ID20160971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57435368..57436168hg38UCSC Ensembl
chr18:55102600..55103400hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118788, nsv1136253
SamplesKWS2, KWS1
Known GenesONECUT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1614n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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