A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003037



Internal ID7068145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45517815..45517910hg38UCSC Ensembl
chr1:45983487..45983582hg19UCSC Ensembl
chr1:45756074..45756169hg18UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3896
hg1996
hg1896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570158
SamplesHuRef
Known GenesPRDX1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003037
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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