A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6090544



Internal ID9586733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96061027..96069361hg38UCSC Ensembl
chr14:96527364..96535698hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388335
hg198335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657868
Supporting Variants
SamplesNA19190
Known GenesC14orf132
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6090544
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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