A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565579



Internal ID6690275
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1009926
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565579
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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