A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565089



Internal ID6689785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12517323..12524706hg38UCSC Ensembl
Outerchr10:12559322..12566705hg19UCSC Ensembl
Outerchr10:12599328..12606711hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387384
hg197384
hg187384
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1011108
Supporting Variants
SamplesHuRef
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565089
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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