A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3437164



Internal ID15284117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33827484..33827516hg38UCSC Ensembl
Innerchr6:33827477..33827521hg38UCSC Ensembl
Outerchr6:33827445..33827555hg38UCSC Ensembl
chr6:33795261..33795293hg19UCSC Ensembl
Innerchr6:33795254..33795298hg19UCSC Ensembl
Outerchr6:33795222..33795332hg19UCSC Ensembl
chr6:33903239..33903271hg18UCSC Ensembl
Innerchr6:33903276..33903232hg18UCSC Ensembl
Outerchr6:33903200..33903310hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381346
hg191346
hg181346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8928908, essv8928904, essv8928906, essv8928905, essv8928907
SamplesNA18870, NA19137, NA19114, NA19093, NA19116
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3437164
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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