A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3574729



Internal ID6699425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48709121..48709443hg38UCSC Ensembl
chr10:49917166..49917488hg19UCSC Ensembl
chr10:49587172..49587494hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38323
hg19323
hg18323
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv999945
Supporting Variants
SamplesHuRef
Known GenesWDFY4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3574729
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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