A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9644603



Internal ID14564150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94948407..94948426hg38UCSC Ensembl
Innerchr9:94948403..94948430hg38UCSC Ensembl
Outerchr9:94948384..94948449hg38UCSC Ensembl
chr9:97710689..97710708hg19UCSC Ensembl
Innerchr9:97710685..97710712hg19UCSC Ensembl
Outerchr9:97710666..97710731hg19UCSC Ensembl
chr9:96750510..96750529hg18UCSC Ensembl
Innerchr9:96750533..96750506hg18UCSC Ensembl
Outerchr9:96750487..96750552hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3368410
Supporting Variants
SamplesNA19141
Known GenesC9orf3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9644603
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