A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621318



Internal ID7008187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103566399..103569568hg38UCSC Ensembl
Innerchr9:103566399..103569568hg38UCSC Ensembl
Outerchr9:103566129..103569830hg38UCSC Ensembl
chr9:106328681..106331850hg19UCSC Ensembl
Innerchr9:106328681..106331850hg19UCSC Ensembl
Outerchr9:106328411..106332112hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg383170
hg193170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13590172, essv13590170, essv13590173, essv13590171
SamplesHG01768, HG01708, HG01775, HG01191
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621318
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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