A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv66e180



Internal ID22757476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27208777..27213647hg38UCSC Ensembl
chr17:25535803..25540673hg19UCSC Ensembl
chr17:22559930..22564800hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg384871
hg194871
hg184871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv1008306, esv996793
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv66e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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