A curated catalogue of human genomic structural variation




Variant Details

Variant: essv84225



Internal ID11650222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105240955..105366526hg38UCSC Ensembl
Innerchr14:105707292..105832863hg19UCSC Ensembl
Innerchr14:104778337..104903908hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38125572
hg19125572
hg18125572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv29986
Supporting Variants
SamplesHuRef
Known GenesBRF1, BTBD6, PACS2
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv84225
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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