A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1570n106



Internal ID22795398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27184836..27185536hg38UCSC Ensembl
chr18:24764800..24765500hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121948, nsv1126479
SamplesKWS2, KWS1
Known GenesCHST9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1570n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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