A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621936



Internal ID6662112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133252403..133258233hg38UCSC Ensembl
Innerchr9:133252404..133258233hg38UCSC Ensembl
Outerchr9:133252403..133258234hg38UCSC Ensembl
chr9:136127790..136133624hg19UCSC Ensembl
Innerchr9:136127791..136133624hg19UCSC Ensembl
Outerchr9:136127790..136133625hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385831
hg195835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13639280, essv13639274, essv13639279, essv13639270, essv13639285, essv13639286, essv13639278, essv13639268, essv13639277, essv13639273, essv13639267, essv13639284, essv13639271, essv13639269, essv13639276, essv13639275, essv13639283, essv13639281, essv13639272, essv13639282
SamplesHG03559, HG03378, HG03074, HG03246, HG02111, HG01369, HG01308, NA18520, NA19152, NA19043, NA19982, HG03446, HG02283, HG03567, NA19375, NA18909, NA19149, NA19102, HG01914, HG01566
Known GenesABO
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621936
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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