A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3438821



Internal ID15285774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33890071..33890124hg38UCSC Ensembl
Innerchr6:33890076..33890119hg38UCSC Ensembl
Outerchr6:33890023..33890172hg38UCSC Ensembl
chr6:33857848..33857901hg19UCSC Ensembl
Innerchr6:33857853..33857896hg19UCSC Ensembl
Outerchr6:33857800..33857949hg19UCSC Ensembl
chr6:33965826..33965879hg18UCSC Ensembl
Innerchr6:33965874..33965831hg18UCSC Ensembl
Outerchr6:33965778..33965927hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38228
hg19228
hg18228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8928910, essv8928913, essv8928912, essv8928911, essv8928909
SamplesNA11995, NA12489, NA12249, NA12716, NA07037
Known GenesLINC01016
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3438821
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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