A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4068428



Internal ID11346760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112526036..112526036hg38UCSC Ensembl
chr9:115288316..115288316hg19UCSC Ensembl
chr9:114328137..114328137hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1674209
Supporting Variants
SamplesHuRef
Known GenesKIAA1958
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4068428
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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