A curated catalogue of human genomic structural variation




Variant Details

Variant: esv987872



Internal ID7075370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:70360006..70361335hg38UCSC Ensembl
Outerchr17:68356147..68357476hg19UCSC Ensembl
Outerchr17:65867742..65869071hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg385786
hg195786
hg185786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564936
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv987872
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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