A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619577



Internal ID7006451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10964906..10971226hg38UCSC Ensembl
Innerchr9:10964913..10971220hg38UCSC Ensembl
Outerchr9:10964900..10971233hg38UCSC Ensembl
chr9:10964906..10971226hg19UCSC Ensembl
Innerchr9:10964913..10971220hg19UCSC Ensembl
Outerchr9:10964900..10971233hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg386321
hg196321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13402647, essv13402650, essv13402649, essv13402648
SamplesNA19700, HG03100, HG03518, NA18984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619577
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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