A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13573620



Internal ID6721078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97244835..97245552hg38UCSC Ensembl
Innerchr9:97244838..97245549hg38UCSC Ensembl
Outerchr9:97244832..97245555hg38UCSC Ensembl
chr9:100007117..100007834hg19UCSC Ensembl
Innerchr9:100007120..100007831hg19UCSC Ensembl
Outerchr9:100007114..100007837hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621187
Supporting Variants
SamplesNA20851
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13573620
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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