A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008898



Internal ID6721005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50253878..50264809hg38UCSC Ensembl
Outerchr3:50291310..50302241hg19UCSC Ensembl
Outerchr3:50266314..50277245hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3810932
hg1910932
hg1810932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565088
SamplesHuRef
Known GenesGNAI2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008898
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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