A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998855



Internal ID7064608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:115968974..115973205hg38UCSC Ensembl
Outerchr10:117728485..117732716hg19UCSC Ensembl
Outerchr10:117718475..117722706hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382790
hg192790
hg182790
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565174
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998855
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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