A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15092904



Internal ID2368166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88879010..88892598hg38UCSC Ensembl
Innerchr14:88879012..88892596hg38UCSC Ensembl
Outerchr14:88879008..88892600hg38UCSC Ensembl
chr14:89345354..89358942hg19UCSC Ensembl
Innerchr14:89345356..89358940hg19UCSC Ensembl
Outerchr14:89345352..89358944hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3813589
hg1913589
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635284
Supporting Variants
SamplesHG02102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15092904
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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