A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1179518



Internal ID11995955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83848184..83848184hg38UCSC Ensembl
chr9:86463099..86463099hg19UCSC Ensembl
chr9:85652919..85652919hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38114
hg19114
hg18114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3982941
SamplesHuRef
Known GenesKIF27
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1179518
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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