A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13618645



Internal ID3287863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124129907..124133492hg38UCSC Ensembl
Innerchr9:124129916..124133484hg38UCSC Ensembl
Outerchr9:124129899..124133501hg38UCSC Ensembl
chr9:126892186..126895771hg19UCSC Ensembl
Innerchr9:126892195..126895763hg19UCSC Ensembl
Outerchr9:126892178..126895780hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383586
hg193586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621711
Supporting Variants
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13618645
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