A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009526



Internal ID7073933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:156993570..157000957hg38UCSC Ensembl
Outerchr5:156420581..156427968hg19UCSC Ensembl
Outerchr5:156353159..156360546hg18UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg387388
hg197388
hg187388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563598
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009526
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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