A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611141



Internal ID6651361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145862268..145862831hg38UCSC Ensembl
Innerchr6:145862318..145862781hg38UCSC Ensembl
Outerchr6:145862218..145862881hg38UCSC Ensembl
chr6:146183404..146183967hg19UCSC Ensembl
Innerchr6:146183454..146183917hg19UCSC Ensembl
Outerchr6:146183354..146184017hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12576890
SamplesNA20522
Known GenesLOC100507557
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611141
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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