A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15109974



Internal ID3276980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102688564..102697445hg38UCSC Ensembl
Innerchr14:102688564..102697445hg38UCSC Ensembl
Outerchr14:102688362..102697613hg38UCSC Ensembl
chr14:103154901..103163782hg19UCSC Ensembl
Innerchr14:103154901..103163782hg19UCSC Ensembl
Outerchr14:103154699..103163950hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg388882
hg198882
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635565
Supporting Variants
SamplesHG02890
Known GenesRCOR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15109974
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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