A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008659



Internal ID6720769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87110988..87111319hg38UCSC Ensembl
chr4:88032140..88032471hg19UCSC Ensembl
chr4:88251164..88251495hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38332
hg19332
hg18332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3581330
SamplesHuRef
Known GenesAFF1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008659
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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