A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620511



Internal ID7007382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42975232..43000118hg38UCSC Ensembl
chr9:66318447..66343333hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3824887
hg1924887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13493906, essv13493905, essv13493903, essv13493907, essv13493908, essv13493904, essv13493902
SamplesHG01054, NA19092, NA12058, HG00641, HG01603, HG01111, NA18740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620511
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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