A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621838



Internal ID7008704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129642396..129643137hg38UCSC Ensembl
Innerchr9:129642396..129643137hg38UCSC Ensembl
Outerchr9:129642087..129643392hg38UCSC Ensembl
chr9:132404675..132405416hg19UCSC Ensembl
Innerchr9:132404675..132405416hg19UCSC Ensembl
Outerchr9:132404366..132405671hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13628414, essv13628415, essv13628416
SamplesNA18605, HG02397, NA19004
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621838
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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