A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5444904



Internal ID9670714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96115194..96115525hg38UCSC Ensembl
chr14:96581531..96581862hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665830
Supporting Variants
SamplesNA19399
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5444904
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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