A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6289693



Internal ID9518110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58100184..58102833hg38UCSC Ensembl
chr14:58566902..58569551hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657771
Supporting Variants
SamplesNA19004
Known GenesC14orf37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6289693
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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