A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611310



Internal ID6651529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154023927..154036131hg38UCSC Ensembl
Innerchr6:154023957..154036101hg38UCSC Ensembl
Outerchr6:154023897..154036161hg38UCSC Ensembl
chr6:154345062..154357266hg19UCSC Ensembl
Innerchr6:154345092..154357236hg19UCSC Ensembl
Outerchr6:154345032..154357296hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3812205
hg1912205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12592326, essv12592324, essv12592325
SamplesNA18563, HG00632, HG02028
Known GenesOPRM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611310
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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