A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1019101



Internal ID11835540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92520065..92520065hg38UCSC Ensembl
chr9:95282347..95282347hg19UCSC Ensembl
chr9:94322168..94322168hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38324
hg19324
hg18324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3787988
SamplesHuRef
Known GenesCENPP, ECM2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1019101
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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