A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8928912



Internal ID13467148
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 StatusS
Merged Variantsesv3438821
Supporting Variants
SamplesNA12489
Known GenesLINC01016
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8928912
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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