A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892552



Internal ID19183372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:60416097..60478741hg38UCSC Ensembl
Outerchr14:60416097..60478741hg38UCSC Ensembl
Innerchr14:60882815..60945459hg19UCSC Ensembl
Outerchr14:60882815..60945459hg19UCSC Ensembl
Innerchr14:59952568..60015212hg18UCSC Ensembl
Outerchr14:59952568..60015212hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3862645
hg1962645
hg1862645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783405
Samples
Known GenesC14orf39
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892552
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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