A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611368



Internal ID6998277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157022715..157032433hg38UCSC Ensembl
Innerchr6:157022718..157032431hg38UCSC Ensembl
Outerchr6:157022713..157032436hg38UCSC Ensembl
chr6:157343849..157353567hg19UCSC Ensembl
Innerchr6:157343852..157353565hg19UCSC Ensembl
Outerchr6:157343847..157353570hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg389719
hg199719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12601132, essv12601133
SamplesHG03478, HG03469
Known GenesARID1B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611368
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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