A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3425333



Internal ID14925604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82903475..82904273hg38UCSC Ensembl
Innerchr4:82903474..82904274hg38UCSC Ensembl
Outerchr4:82902475..82905273hg38UCSC Ensembl
chr4:83824628..83825426hg19UCSC Ensembl
Innerchr4:83824627..83825427hg19UCSC Ensembl
Outerchr4:83823628..83826426hg19UCSC Ensembl
chr4:84043652..84044450hg18UCSC Ensembl
Innerchr4:84044451..84043651hg18UCSC Ensembl
Outerchr4:84042652..84045450hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8694519
SamplesNA19240
Known GenesTHAP9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3425333
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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