A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990725



Internal ID7076856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:2758272..2771034hg38UCSC Ensembl
Outerchr2:2762044..2774806hg19UCSC Ensembl
Outerchr2:2741051..2753813hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3812763
hg1912763
hg1812763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563633
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990725
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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