A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999925



Internal ID6735848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25469705..25469761hg38UCSC Ensembl
chr8:25327221..25327277hg19UCSC Ensembl
chr8:25383138..25383194hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3573240
SamplesHuRef
Known GenesCDCA2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999925
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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