A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009926



Internal ID6722018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76246661..76256546hg38UCSC Ensembl
Outerchr17:74242742..74252627hg19UCSC Ensembl
Outerchr17:71754337..71764222hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg389886
hg199886
hg189886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565579
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009926
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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