A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9667447



Internal ID13605761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94558259..94558278hg38UCSC Ensembl
Innerchr14:94558255..94558282hg38UCSC Ensembl
Outerchr14:94558236..94558301hg38UCSC Ensembl
chr14:95024596..95024615hg19UCSC Ensembl
Innerchr14:95024592..95024619hg19UCSC Ensembl
Outerchr14:95024573..95024638hg19UCSC Ensembl
chr14:94094349..94094368hg18UCSC Ensembl
Innerchr14:94094372..94094345hg18UCSC Ensembl
Outerchr14:94094326..94094391hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3324868
Supporting Variants
SamplesNA12815
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9667447
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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