A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621712



Internal ID7008579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124144900..124153442hg38UCSC Ensembl
Innerchr9:124144900..124153442hg38UCSC Ensembl
Outerchr9:124144662..124153784hg38UCSC Ensembl
chr9:126907179..126915721hg19UCSC Ensembl
Innerchr9:126907179..126915721hg19UCSC Ensembl
Outerchr9:126906941..126916063hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg388543
hg198543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618651, essv13618649, essv13618652, essv13618650, essv13618648
SamplesNA18959, NA19059, NA18941, NA19085, NA19011
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621712
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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