A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621295



Internal ID7008164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102841927..102899804hg38UCSC Ensembl
Innerchr9:102841927..102899804hg38UCSC Ensembl
Outerchr9:102841427..102900304hg38UCSC Ensembl
chr9:105604209..105662086hg19UCSC Ensembl
Innerchr9:105604209..105662086hg19UCSC Ensembl
Outerchr9:105603709..105662586hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3857878
hg1957878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13588133
SamplesHG01485
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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