A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13407123



Internal ID6710519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14542296..14551168hg38UCSC Ensembl
Innerchr9:14542296..14551168hg38UCSC Ensembl
Outerchr9:14542028..14551214hg38UCSC Ensembl
chr9:14542294..14551166hg19UCSC Ensembl
Innerchr9:14542294..14551166hg19UCSC Ensembl
Outerchr9:14542026..14551212hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg388873
hg198873
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619751
Supporting Variants
SamplesNA20846
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13407123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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