A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3360429



Internal ID15207408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19730504..19730504hg38UCSC Ensembl
Innerchr6:19730503..19730505hg38UCSC Ensembl
Outerchr6:19730444..19730554hg38UCSC Ensembl
chr6:19730735..19730735hg19UCSC Ensembl
Innerchr6:19730734..19730736hg19UCSC Ensembl
Outerchr6:19730675..19730785hg19UCSC Ensembl
chr6:19838714..19838714hg18UCSC Ensembl
Innerchr6:19838715..19838713hg18UCSC Ensembl
Outerchr6:19838654..19838764hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3865
hg1965
hg1865
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8839012
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3360429
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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