A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13601807



Internal ID3603623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111403383..111407448hg38UCSC Ensembl
Innerchr9:111403384..111407448hg38UCSC Ensembl
Outerchr9:111403383..111407449hg38UCSC Ensembl
chr9:114165663..114169728hg19UCSC Ensembl
Innerchr9:114165664..114169728hg19UCSC Ensembl
Outerchr9:114165663..114169729hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg384066
hg194066
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621488
Supporting Variants
SamplesHG03136
Known GenesKIAA0368
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13601807
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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