A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1581n106



Internal ID22795409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39800836..39803336hg38UCSC Ensembl
chr18:37380800..37383300hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1128771, nsv1115532
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1581n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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