A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3351848



Internal ID15198829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158249337..158249356hg38UCSC Ensembl
Innerchr6:158249333..158249360hg38UCSC Ensembl
Outerchr6:158249314..158249379hg38UCSC Ensembl
chr6:158670369..158670388hg19UCSC Ensembl
Innerchr6:158670365..158670392hg19UCSC Ensembl
Outerchr6:158670346..158670411hg19UCSC Ensembl
chr6:158590357..158590376hg18UCSC Ensembl
Innerchr6:158590380..158590353hg18UCSC Ensembl
Outerchr6:158590334..158590399hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9631980
SamplesNA12234
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3351848
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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