A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5921204



Internal ID9535552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34786653..34788038hg38UCSC Ensembl
Outerchr14:34786616..34788088hg38UCSC Ensembl
Innerchr14:35255859..35257244hg19UCSC Ensembl
Outerchr14:35255822..35257294hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661600
Supporting Variants
SamplesNA19065
Known GenesBAZ1A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5921204
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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