A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302700



Internal ID15149648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101419834..101420157hg38UCSC Ensembl
Innerchr9:101419934..101420057hg38UCSC Ensembl
Outerchr9:101419734..101420257hg38UCSC Ensembl
chr9:104182116..104182439hg19UCSC Ensembl
Innerchr9:104182216..104182339hg19UCSC Ensembl
Outerchr9:104182016..104182539hg19UCSC Ensembl
chr9:103221937..103222260hg18UCSC Ensembl
Innerchr9:103222037..103222160hg18UCSC Ensembl
Outerchr9:103221837..103222360hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38324
hg19324
hg18324
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7737301, essv7738203, essv7736418, essv7735853, essv7733318, essv7734352, essv7731763, essv7736888, essv7733962, essv7737689, essv7735710
SamplesNA11830, NA10851, NA12045, NA12751, NA12287, NA19138, NA19172, NA12828, NA07037, NA06986, NA07000
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302700
Frequency
Sample Size185
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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