A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3425923



Internal ID15272880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86968906..86968926hg38UCSC Ensembl
Innerchr6:86968905..86968924hg38UCSC Ensembl
Outerchr6:86968885..86968944hg38UCSC Ensembl
chr6:87678624..87678644hg19UCSC Ensembl
Innerchr6:87678623..87678642hg19UCSC Ensembl
Outerchr6:87678603..87678662hg19UCSC Ensembl
chr6:87735343..87735363hg18UCSC Ensembl
Innerchr6:87735361..87735342hg18UCSC Ensembl
Outerchr6:87735322..87735381hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38288
hg19288
hg18288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8931151, essv8931147, essv8931149, essv8931153, essv8931155, essv8931150, essv8931146, essv8931152, essv8931154
SamplesNA12004, NA07346, NA18944, NA12156, NA11994, NA18605, NA18593, NA11881, NA07051
Known GenesHTR1E
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3425923
Frequency
Sample Size185
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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