A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621834



Internal ID7008700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129540936..129547578hg38UCSC Ensembl
Innerchr9:129540937..129547577hg38UCSC Ensembl
Outerchr9:129540935..129547579hg38UCSC Ensembl
chr9:132303215..132309857hg19UCSC Ensembl
Innerchr9:132303216..132309856hg19UCSC Ensembl
Outerchr9:132303214..132309858hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386643
hg196643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13628374, essv13628373, essv13628375
SamplesHG00121, HG02490, HG02233
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621834
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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