A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621430



Internal ID6661609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109143603..109144777hg38UCSC Ensembl
Innerchr9:109143638..109144742hg38UCSC Ensembl
Outerchr9:109143568..109144812hg38UCSC Ensembl
chr9:111905883..111907057hg19UCSC Ensembl
Innerchr9:111905918..111907022hg19UCSC Ensembl
Outerchr9:111905848..111907092hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13595269, essv13595265, essv13595268, essv13595266, essv13595267, essv13595264, essv13595273, essv13595274, essv13595270, essv13595263, essv13595272, essv13595271
SamplesNA19332, NA19377, HG02810, NA19923, HG03045, NA19385, NA19043, NA19436, NA19308, HG02464, HG02343, HG03166
Known GenesFRRS1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621430
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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