A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13493902



Internal ID1024799
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620511
Supporting Variants
SamplesHG00641
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13493902
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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