A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4012665



Internal ID11402522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86999017..86999017hg38UCSC Ensembl
chr9:89613932..89613932hg19UCSC Ensembl
chr9:88803752..88803752hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382433
hg192433
hg182433
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1694845
Supporting Variants
SamplesHuRef
Known GenesLOC100506834
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4012665
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer