A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3309609



Internal ID15156560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99023480..99023481hg38UCSC Ensembl
Innerchr6:99023448..99023513hg38UCSC Ensembl
Outerchr6:99023447..99023514hg38UCSC Ensembl
chr6:99471356..99471357hg19UCSC Ensembl
Innerchr6:99471324..99471389hg19UCSC Ensembl
Outerchr6:99471323..99471390hg19UCSC Ensembl
chr6:99578077..99578078hg18UCSC Ensembl
Innerchr6:99578110..99578045hg18UCSC Ensembl
Outerchr6:99578044..99578111hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38169
hg19169
hg18169
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7838686, essv7837702, essv7836752
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3309609
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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