A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621137



Internal ID6661317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94735219..94750968hg38UCSC Ensembl
Innerchr9:94735719..94750468hg38UCSC Ensembl
Outerchr9:94734219..94751968hg38UCSC Ensembl
chr9:97497501..97513250hg19UCSC Ensembl
Innerchr9:97498001..97512750hg19UCSC Ensembl
Outerchr9:97496501..97514250hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3815750
hg1915750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13571498
SamplesHG00739
Known GenesC9orf3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621137
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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