A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4028406



Internal ID11733468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154125795..154126117hg38UCSC Ensembl
chr6:154446930..154447252hg19UCSC Ensembl
chr6:154488622..154488944hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38323
hg19323
hg18323
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1146800
Supporting Variants
SamplesHuRef
Known GenesOPRM1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4028406
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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