A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620716



Internal ID7007586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75190493..75199089hg38UCSC Ensembl
Innerchr9:75190493..75199089hg38UCSC Ensembl
Outerchr9:75190343..75199322hg38UCSC Ensembl
chr9:77805409..77814005hg19UCSC Ensembl
Innerchr9:77805409..77814005hg19UCSC Ensembl
Outerchr9:77805259..77814238hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388597
hg198597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13526642, essv13526638, essv13526632, essv13526644, essv13526641, essv13526636, essv13526633, essv13526637, essv13526639, essv13526635, essv13526634, essv13526643, essv13526640, essv13526631
SamplesHG04210, HG04076, NA20896, HG04106, NA21107, HG03750, HG03784, NA21119, HG03636, NA20862, HG02604, HG04227, NA20897, NA21090
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620716
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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