A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586768



Internal ID6711464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77492849..77493574hg38UCSC Ensembl
Innerchr17:75488931..75489656hg19UCSC Ensembl
Innerchr17:73000526..73001251hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38726
hg19726
hg18726
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1001835
Supporting Variants
SamplesHuRef
Known GenesSEPT9
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586768
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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