A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1661n106



Internal ID20161018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79739737..79740226hg38UCSC Ensembl
chr18:77499737..77500226hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135845, nsv1140319
SamplesKWS1, KWS2
Known GenesCTDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1661n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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