A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3427615



Internal ID15274571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36763355..36764853hg38UCSC Ensembl
Innerchr9:36763853..36764355hg38UCSC Ensembl
Outerchr9:36762355..36765853hg38UCSC Ensembl
chr9:36763352..36764850hg19UCSC Ensembl
Innerchr9:36763850..36764352hg19UCSC Ensembl
Outerchr9:36762352..36765850hg19UCSC Ensembl
chr9:36753352..36754850hg18UCSC Ensembl
Innerchr9:36754352..36753850hg18UCSC Ensembl
Outerchr9:36752352..36755850hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696621
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3427615
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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