A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1552n106



Internal ID19019661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11826269..11826399hg38UCSC Ensembl
chr18:11826268..11826398hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126325, nsv1112176
SamplesKWS1
Known GenesGNAL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1552n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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