A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565367



Internal ID7036749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:37704906..37718494hg38UCSC Ensembl
Outerchr6:37672682..37686270hg19UCSC Ensembl
Outerchr6:37780660..37794248hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3813589
hg1913589
hg1813589
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994460
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565367
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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