A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3339562



Internal ID15186549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160915399..160915418hg38UCSC Ensembl
Innerchr6:160915395..160915422hg38UCSC Ensembl
Outerchr6:160915376..160915441hg38UCSC Ensembl
chr6:161336431..161336450hg19UCSC Ensembl
Innerchr6:161336427..161336454hg19UCSC Ensembl
Outerchr6:161336408..161336473hg19UCSC Ensembl
chr6:161256421..161256440hg18UCSC Ensembl
Innerchr6:161256444..161256417hg18UCSC Ensembl
Outerchr6:161256398..161256463hg18UCSC Ensembl
Cytoband6q26
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 Variantsessv9632091
SamplesNA12234
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3339562
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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