A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15114230



Internal ID4995740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103261875..103270675hg38UCSC Ensembl
Innerchr14:103261925..103270625hg38UCSC Ensembl
Outerchr14:103261825..103270725hg38UCSC Ensembl
chr14:103728212..103737012hg19UCSC Ensembl
Innerchr14:103728262..103736962hg19UCSC Ensembl
Outerchr14:103728162..103737062hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg388801
hg198801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635584
Supporting Variants
SamplesNA18499
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15114230
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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