A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12592325



Internal ID2594141
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611310
Supporting Variants
SamplesHG02028
Known GenesOPRM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12592325
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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