A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3369019



Internal ID15215995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11588744..11588744hg38UCSC Ensembl
Innerchr6:11588743..11588745hg38UCSC Ensembl
Outerchr6:11588684..11588794hg38UCSC Ensembl
chr6:11588977..11588977hg19UCSC Ensembl
Innerchr6:11588976..11588978hg19UCSC Ensembl
Outerchr6:11588917..11589027hg19UCSC Ensembl
chr6:11696963..11696963hg18UCSC Ensembl
Innerchr6:11696964..11696962hg18UCSC Ensembl
Outerchr6:11696903..11697013hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3870
hg1970
hg1870
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8837326
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3369019
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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