A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564098



Internal ID7035198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:68993337..68994285hg38UCSC Ensembl
Outerchr10:70753093..70754041hg19UCSC Ensembl
Outerchr10:70423099..70424047hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384278
hg194278
hg184278
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000949
Supporting Variants
SamplesHuRef
Known GenesKIAA1279
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564098
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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