A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4196897



Internal ID11479435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113111681..113112890hg38UCSC Ensembl
chr9:115873961..115875170hg19UCSC Ensembl
chr9:114913782..114914991hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381210
hg191210
hg181210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1720272
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4196897
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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