A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5723881



Internal ID9749569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102156035..102164204hg38UCSC Ensembl
chr14:102622372..102630541hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg388170
hg198170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678767
Supporting Variants
SamplesNA19700
Known GenesWDR20
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5723881
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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