A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv128n97



Internal ID22815525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18390113..18592992hg38UCSC Ensembl
chr17:18293427..18496306hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38202880
hg19202880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155390, nsv1155388, nsv1155389
Samples
Known GenesCCDC144B, FAM106A, FLJ35934, KRT16P1, LGALS9C, LOC339240, USP32P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv128n97
Frequency
Sample Size131
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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