A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611277



Internal ID6651496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151984276..151985418hg38UCSC Ensembl
Innerchr6:151984321..151985374hg38UCSC Ensembl
Outerchr6:151984232..151985463hg38UCSC Ensembl
chr6:152305411..152306553hg19UCSC Ensembl
Innerchr6:152305456..152306509hg19UCSC Ensembl
Outerchr6:152305367..152306598hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12585033, essv12585032, essv12585030, essv12585031, essv12585028, essv12585029
SamplesHG01242, NA19035, NA18571, NA19315, HG03449, NA19113
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611277
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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