A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13406253



Internal ID1561014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13300222..13325794hg38UCSC Ensembl
Innerchr9:13300222..13325794hg38UCSC Ensembl
Outerchr9:13299722..13326294hg38UCSC Ensembl
chr9:13300221..13325793hg19UCSC Ensembl
Innerchr9:13300221..13325793hg19UCSC Ensembl
Outerchr9:13299721..13326293hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3825573
hg1925573
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619729
Supporting Variants
SamplesHG01441
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13406253
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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