A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15109995



Internal ID5111811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102794071..102797944hg38UCSC Ensembl
Innerchr14:102794121..102797894hg38UCSC Ensembl
Outerchr14:102794021..102797994hg38UCSC Ensembl
chr14:103260408..103264281hg19UCSC Ensembl
Innerchr14:103260458..103264231hg19UCSC Ensembl
Outerchr14:103260358..103264331hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg383874
hg193874
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635572
Supporting Variants
SamplesHG03858
Known GenesTRAF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15109995
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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