A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621039



Internal ID7007909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90037283..90040849hg38UCSC Ensembl
Innerchr9:90037284..90040848hg38UCSC Ensembl
Outerchr9:90037282..90040850hg38UCSC Ensembl
chr9:92799565..92803131hg19UCSC Ensembl
Innerchr9:92799566..92803130hg19UCSC Ensembl
Outerchr9:92799564..92803132hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg383567
hg193567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13552297
SamplesHG01137
Known GenesLOC286370
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621039
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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