A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3336017



Internal ID15183006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95425920..95425920hg38UCSC Ensembl
Innerchr6:95425919..95425921hg38UCSC Ensembl
Outerchr6:95425870..95425970hg38UCSC Ensembl
chr6:95873796..95873796hg19UCSC Ensembl
Innerchr6:95873795..95873797hg19UCSC Ensembl
Outerchr6:95873746..95873846hg19UCSC Ensembl
chr6:95980517..95980517hg18UCSC Ensembl
Innerchr6:95980518..95980516hg18UCSC Ensembl
Outerchr6:95980467..95980567hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381442
hg191442
hg181442
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8741268
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3336017
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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