A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13552297



Internal ID1298998
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621039
Supporting Variants
SamplesHG01137
Known GenesLOC286370
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13552297
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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