A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3568554



Internal ID6693250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154125788..154126109hg38UCSC Ensembl
chr6:154446923..154447244hg19UCSC Ensembl
chr6:154488615..154488936hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38322
hg19322
hg18322
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000500
Supporting Variants
SamplesHuRef
Known GenesOPRM1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3568554
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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