A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621015



Internal ID7007885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88902784..88911492hg38UCSC Ensembl
Innerchr9:88902815..88911461hg38UCSC Ensembl
Outerchr9:88902753..88911523hg38UCSC Ensembl
chr9:91517699..91526407hg19UCSC Ensembl
Innerchr9:91517730..91526376hg19UCSC Ensembl
Outerchr9:91517668..91526438hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg388709
hg198709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13549494, essv13549493
SamplesHG01513, NA12830
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621015
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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