A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620645



Internal ID7007515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72646167..72649179hg38UCSC Ensembl
Innerchr9:72646181..72649165hg38UCSC Ensembl
Outerchr9:72646153..72649193hg38UCSC Ensembl
chr9:75261083..75264095hg19UCSC Ensembl
Innerchr9:75261097..75264081hg19UCSC Ensembl
Outerchr9:75261069..75264109hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383013
hg193013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13516721
SamplesHG00178
Known GenesTMC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620645
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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