A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15114591



Internal ID2031027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103851243..103851821hg38UCSC Ensembl
Innerchr14:103851293..103851771hg38UCSC Ensembl
Outerchr14:103851163..103851901hg38UCSC Ensembl
chr14:104317580..104318158hg19UCSC Ensembl
Innerchr14:104317630..104318108hg19UCSC Ensembl
Outerchr14:104317500..104318238hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635610
Supporting Variants
SamplesHG01864
Known GenesLINC00637
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15114591
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer