A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13602876



Internal ID2585869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111963570..111964589hg38UCSC Ensembl
Innerchr9:111963570..111964589hg38UCSC Ensembl
Outerchr9:111963203..111965103hg38UCSC Ensembl
chr9:114725850..114726869hg19UCSC Ensembl
Innerchr9:114725850..114726869hg19UCSC Ensembl
Outerchr9:114725483..114727383hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621498
Supporting Variants
SamplesHG02286
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13602876
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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