A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001563



Internal ID7066687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183731928..183739129hg38UCSC Ensembl
Outerchr4:184653081..184660282hg19UCSC Ensembl
Outerchr4:184890075..184897276hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg387202
hg197202
hg187202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563741
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001563
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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