A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865740



Internal ID13863687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59370144..59370160hg38UCSC Ensembl
Innerchr14:59370146..59370158hg38UCSC Ensembl
Outerchr14:59370142..59370162hg38UCSC Ensembl
chr14:59836862..59836878hg19UCSC Ensembl
Innerchr14:59836864..59836876hg19UCSC Ensembl
Outerchr14:59836860..59836880hg19UCSC Ensembl
chr14:58906615..58906631hg18UCSC Ensembl
Innerchr14:58906617..58906629hg18UCSC Ensembl
Outerchr14:58906613..58906633hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3409729
Supporting Variants
SamplesNA18516
Known GenesDAAM1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865740
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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