A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621830



Internal ID7008696
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13628317, essv13628308, essv13628320, essv13628318, essv13628305, essv13628316, essv13628307, essv13628310, essv13628319, essv13628322, essv13628315, essv13628306, essv13628309, essv13628312, essv13628313, essv13628314, essv13628311, essv13628321
SamplesNA19394, NA19914, HG03449, NA19355, NA19190, HG03436, NA19131, NA19197, HG03380, NA18520, NA18516, HG03085, NA18909, HG02546, HG03433, HG02814, HG02855, NA19316
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621830
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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