A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564851



Internal ID7035951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:86503339..86504953hg38UCSC Ensembl
Outerchr10:88263096..88264710hg19UCSC Ensembl
Outerchr10:88253076..88254690hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg383553
hg193553
hg183553
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003241
Supporting Variants
SamplesHuRef
Known GenesWAPAL
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564851
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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