A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611373



Internal ID6998282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157121848..157122917hg38UCSC Ensembl
Innerchr6:157121848..157122917hg38UCSC Ensembl
Outerchr6:157121512..157123220hg38UCSC Ensembl
chr6:157442982..157444051hg19UCSC Ensembl
Innerchr6:157442982..157444051hg19UCSC Ensembl
Outerchr6:157442646..157444354hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12601517, essv12601518, essv12601516
SamplesHG01989, HG03354, HG04227
Known GenesARID1B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611373
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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