A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13628307



Internal ID3241808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129358677..129359191hg38UCSC Ensembl
Innerchr9:129358677..129359191hg38UCSC Ensembl
Outerchr9:129358357..129359448hg38UCSC Ensembl
chr9:132120956..132121470hg19UCSC Ensembl
Innerchr9:132120956..132121470hg19UCSC Ensembl
Outerchr9:132120636..132121727hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621830
Supporting Variants
SamplesHG02855
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13628307
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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