A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586901



Internal ID7058283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34874613..34875272hg38UCSC Ensembl
Innerchr14:35343819..35344478hg19UCSC Ensembl
Innerchr14:34413570..34414229hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38660
hg19660
hg18660
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006744
Supporting Variants
SamplesHuRef
Known GenesBAZ1A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586901
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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