A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697122



Internal ID15060879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63315060..63335458hg38UCSC Ensembl
Innerchr9:63316060..63334458hg38UCSC Ensembl
Outerchr9:63314060..63336458hg38UCSC Ensembl
chr9:67270032..67290430hg19UCSC Ensembl
Innerchr9:67271032..67289430hg19UCSC Ensembl
Outerchr9:67269032..67291430hg19UCSC Ensembl
chr9:66959852..66980250hg18UCSC Ensembl
Innerchr9:66960852..66979250hg18UCSC Ensembl
Outerchr9:66958852..66981250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820399
hg1920399
hg1820399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3410639
Supporting Variants
SamplesNA19239
Known GenesAQP7P1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697122
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