A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621112



Internal ID7007981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94149587..94155411hg38UCSC Ensembl
Innerchr9:94149610..94155389hg38UCSC Ensembl
Outerchr9:94149565..94155434hg38UCSC Ensembl
chr9:96911869..96917693hg19UCSC Ensembl
Innerchr9:96911892..96917671hg19UCSC Ensembl
Outerchr9:96911847..96917716hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385825
hg195825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13567288
SamplesNA20762
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621112
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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