A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611190



Internal ID6998101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148361770..148371451hg38UCSC Ensembl
Innerchr6:148362270..148370951hg38UCSC Ensembl
Outerchr6:148360770..148372451hg38UCSC Ensembl
chr6:148682906..148692587hg19UCSC Ensembl
Innerchr6:148683406..148692087hg19UCSC Ensembl
Outerchr6:148681906..148693587hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg389682
hg199682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12579750
SamplesHG01405
Known GenesSASH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611190
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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