A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620293



Internal ID6660477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32295271..32308676hg38UCSC Ensembl
Innerchr9:32295280..32308667hg38UCSC Ensembl
Outerchr9:32295262..32308685hg38UCSC Ensembl
chr9:32295269..32308674hg19UCSC Ensembl
Innerchr9:32295278..32308665hg19UCSC Ensembl
Outerchr9:32295260..32308683hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3813406
hg1913406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13449245
SamplesNA20763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620293
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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