A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29987



Internal ID12954867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:269735..349386hg38UCSC Ensembl
Innerchr6:269735..349386hg19UCSC Ensembl
Innerchr6:214735..294386hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3879652
hg1979652
hg1879652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84226
SamplesHuRef
Known GenesDUSP22
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29987
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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