A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007603



Internal ID6719716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13489372..13500710hg38UCSC Ensembl
Outerchr10:13531372..13542710hg19UCSC Ensembl
Outerchr10:13571378..13582716hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3811339
hg1911339
hg1811339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564046
SamplesHuRef
Known GenesBEND7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007603
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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