A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8695071



Internal ID14703861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159914330..159916428hg38UCSC Ensembl
Innerchr6:159915330..159915428hg38UCSC Ensembl
Outerchr6:159913330..159917428hg38UCSC Ensembl
chr6:160335362..160337460hg19UCSC Ensembl
Innerchr6:160336362..160336460hg19UCSC Ensembl
Outerchr6:160334362..160338460hg19UCSC Ensembl
chr6:160255352..160257450hg18UCSC Ensembl
Innerchr6:160256352..160256450hg18UCSC Ensembl
Outerchr6:160254352..160258450hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3418081
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8695071
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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