A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3353333



Internal ID15200314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1897919..1898217hg38UCSC Ensembl
Innerchr6:1897918..1898218hg38UCSC Ensembl
Outerchr6:1896919..1899217hg38UCSC Ensembl
chr6:1898153..1898451hg19UCSC Ensembl
Innerchr6:1898152..1898452hg19UCSC Ensembl
Outerchr6:1897153..1899451hg19UCSC Ensembl
chr6:1843152..1843450hg18UCSC Ensembl
Innerchr6:1843451..1843151hg18UCSC Ensembl
Outerchr6:1842152..1844450hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38299
hg19299
hg18299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695180
SamplesNA19239
Known GenesGMDS
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3353333
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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