A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13607923



Internal ID3343782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114938211..114940609hg38UCSC Ensembl
Innerchr9:114938211..114940609hg38UCSC Ensembl
Outerchr9:114938086..114940758hg38UCSC Ensembl
chr9:117700491..117702889hg19UCSC Ensembl
Innerchr9:117700491..117702889hg19UCSC Ensembl
Outerchr9:117700366..117703038hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382399
hg192399
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621564
Supporting Variants
SamplesHG02981
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13607923
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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