A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621341



Internal ID7008210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104717697..104729043hg38UCSC Ensembl
Innerchr9:104717726..104729014hg38UCSC Ensembl
Outerchr9:104717668..104729072hg38UCSC Ensembl
chr9:107479978..107491324hg19UCSC Ensembl
Innerchr9:107480007..107491295hg19UCSC Ensembl
Outerchr9:107479949..107491353hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3811347
hg1911347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13591897, essv13591898, essv13591902, essv13591900, essv13591894, essv13591895, essv13591899, essv13591903, essv13591901, essv13591896
SamplesNA12273, HG00151, NA12283, HG00355, HG02008, HG00265, HG00375, NA12873, HG00123, NA07000
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621341
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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