A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13612836



Internal ID5609430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118816609..118822086hg38UCSC Ensembl
Innerchr9:118816620..118822076hg38UCSC Ensembl
Outerchr9:118816599..118822097hg38UCSC Ensembl
chr9:121578887..121584364hg19UCSC Ensembl
Innerchr9:121578898..121584354hg19UCSC Ensembl
Outerchr9:121578877..121584375hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg385478
hg195478
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621627
Supporting Variants
SamplesNA19038
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13612836
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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