A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3384480



Internal ID15231450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101123103..101123122hg38UCSC Ensembl
Innerchr9:101123099..101123126hg38UCSC Ensembl
Outerchr9:101123080..101123145hg38UCSC Ensembl
chr9:103885385..103885404hg19UCSC Ensembl
Innerchr9:103885381..103885408hg19UCSC Ensembl
Outerchr9:103885362..103885427hg19UCSC Ensembl
chr9:102925206..102925225hg18UCSC Ensembl
Innerchr9:102925229..102925202hg18UCSC Ensembl
Outerchr9:102925183..102925248hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9644769
SamplesNA18970
Known GenesLPPR1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3384480
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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