A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621926



Internal ID6662102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132884570..132886716hg38UCSC Ensembl
Innerchr9:132884570..132886716hg38UCSC Ensembl
Outerchr9:132884431..132886781hg38UCSC Ensembl
chr9:135759957..135762103hg19UCSC Ensembl
Innerchr9:135759957..135762103hg19UCSC Ensembl
Outerchr9:135759818..135762168hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13638529
SamplesHG03838
Known GenesC9orf9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621926
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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