A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586832



Internal ID7058214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57692761..57694411hg38UCSC Ensembl
Innerchr10:59452521..59454171hg19UCSC Ensembl
Innerchr10:59122527..59124177hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381651
hg191651
hg181651
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000733
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586832
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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