A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620652



Internal ID7007522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72839049..72850479hg38UCSC Ensembl
Innerchr9:72839049..72850479hg38UCSC Ensembl
Outerchr9:72838549..72850979hg38UCSC Ensembl
chr9:75453965..75465395hg19UCSC Ensembl
Innerchr9:75453965..75465395hg19UCSC Ensembl
Outerchr9:75453465..75465895hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3811431
hg1911431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13517107
SamplesNA20864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620652
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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