A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621745



Internal ID7008611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125393126..125399969hg38UCSC Ensembl
Innerchr9:125393143..125399953hg38UCSC Ensembl
Outerchr9:125393110..125399986hg38UCSC Ensembl
chr9:128155405..128162248hg19UCSC Ensembl
Innerchr9:128155422..128162232hg19UCSC Ensembl
Outerchr9:128155389..128162265hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386844
hg196844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618977, essv13618976
SamplesNA19917, NA06986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621745
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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