A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13415189



Internal ID3210466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18833106..18856929hg38UCSC Ensembl
chr9:18833104..18856927hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3823824
hg1923824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619883
Supporting Variants
SamplesHG02816
Known GenesADAMTSL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13415189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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