A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3409018



Internal ID15255979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33923797..33925395hg38UCSC Ensembl
Innerchr6:33924395..33924797hg38UCSC Ensembl
Outerchr6:33922797..33926395hg38UCSC Ensembl
chr6:33891574..33893172hg19UCSC Ensembl
Innerchr6:33892172..33892574hg19UCSC Ensembl
Outerchr6:33890574..33894172hg19UCSC Ensembl
chr6:33999552..34001150hg18UCSC Ensembl
Innerchr6:34000552..34000150hg18UCSC Ensembl
Outerchr6:33998552..34002150hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695277
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3409018
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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