A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15109990



Internal ID908472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102768351..102769206hg38UCSC Ensembl
Innerchr14:102768351..102769206hg38UCSC Ensembl
Outerchr14:102768063..102769494hg38UCSC Ensembl
chr14:103234688..103235543hg19UCSC Ensembl
Innerchr14:103234688..103235543hg19UCSC Ensembl
Outerchr14:103234400..103235831hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635570
Supporting Variants
SamplesHG00533
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15109990
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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