A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996048



Internal ID6731995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62868221..62868854hg38UCSC Ensembl
Innerchr17:60945582..60946215hg19UCSC Ensembl
Innerchr17:58299314..58299947hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38634
hg19634
hg18634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586830
SamplesHuRef
Known GenesMIR548W
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996048
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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