A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621953



Internal ID7008819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134167403..134169197hg38UCSC Ensembl
Innerchr9:134167403..134169197hg38UCSC Ensembl
Outerchr9:134167159..134169456hg38UCSC Ensembl
chr9:137032525..137034319hg19UCSC Ensembl
Innerchr9:137032525..137034319hg19UCSC Ensembl
Outerchr9:137032281..137034578hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381795
hg191795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13641422, essv13641420, essv13641411, essv13641423, essv13641419, essv13641417, essv13641424, essv13641414, essv13641428, essv13641427, essv13641425, essv13641412, essv13641415, essv13641421, essv13641418, essv13641416, essv13641426, essv13641410, essv13641413
SamplesHG03175, HG03111, HG03172, HG01461, HG03372, NA18510, NA19171, HG02111, HG02571, HG03160, NA18933, NA19982, HG03159, HG02508, NA19108, HG02501, NA19102, NA19096, HG03129
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621953
Frequency
Sample Size2504
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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