A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2992526



Internal ID10665506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45517804..45517911hg38UCSC Ensembl
chr1:45983476..45983583hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7262093
SamplesHuRef
Known GenesPRDX1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2992526
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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