A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3445329



Internal ID15292281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110493945..110493964hg38UCSC Ensembl
Innerchr6:110493941..110493968hg38UCSC Ensembl
Outerchr6:110493922..110493987hg38UCSC Ensembl
chr6:110815148..110815167hg19UCSC Ensembl
Innerchr6:110815144..110815171hg19UCSC Ensembl
Outerchr6:110815125..110815190hg19UCSC Ensembl
chr6:110921841..110921860hg18UCSC Ensembl
Innerchr6:110921864..110921837hg18UCSC Ensembl
Outerchr6:110921818..110921883hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9630337
SamplesNA12249
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3445329
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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