A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8694196



Internal ID15010909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108397047..108398345hg38UCSC Ensembl
Innerchr4:108397345..108398047hg38UCSC Ensembl
Outerchr4:108396047..108399345hg38UCSC Ensembl
chr4:109318203..109319501hg19UCSC Ensembl
Innerchr4:109318501..109319203hg19UCSC Ensembl
Outerchr4:109317203..109320501hg19UCSC Ensembl
chr4:109537652..109538950hg18UCSC Ensembl
Innerchr4:109538652..109537950hg18UCSC Ensembl
Outerchr4:109536652..109539950hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3380149
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8694196
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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