A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003773



Internal ID6715900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201685221..201685289hg38UCSC Ensembl
chr2:202549944..202550012hg19UCSC Ensembl
chr2:202258189..202258257hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3581292
SamplesHuRef
Known GenesMPP4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003773
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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