A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1557n106



Internal ID22795385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:20931240..20937132hg38UCSC Ensembl
chr18:18511201..18517093hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg385893
hg195893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135835, nsv1116473
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1557n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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