A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9626014



Internal ID13175117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13718226..13718245hg38UCSC Ensembl
Innerchr6:13718222..13718249hg38UCSC Ensembl
Outerchr6:13718203..13718268hg38UCSC Ensembl
chr6:13718458..13718477hg19UCSC Ensembl
Innerchr6:13718454..13718481hg19UCSC Ensembl
Outerchr6:13718435..13718500hg19UCSC Ensembl
chr6:13826437..13826456hg18UCSC Ensembl
Innerchr6:13826460..13826433hg18UCSC Ensembl
Outerchr6:13826414..13826479hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3356094
Supporting Variants
SamplesNA11881
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9626014
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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